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http://purl.uniprot.org/citations/10862102http://www.w3.org/1999/02/22-rdf-syntax-ns#typehttp://purl.uniprot.org/core/Journal_Citation
http://purl.uniprot.org/citations/10862102http://www.w3.org/1999/02/22-rdf-syntax-ns#typehttp://purl.uniprot.org/core/Journal_Citation
http://purl.uniprot.org/citations/10862102http://purl.org/dc/terms/identifier"doi:10.1002/1098-1004(200006)15:6<584::aid-humu25>3.0.co;2-r"xsd:string
http://purl.uniprot.org/citations/10862102http://purl.org/dc/terms/identifier"doi:10.1002/1098-1004(200006)15:6<584::aid-humu25>3.0.co;2-r"xsd:string
http://purl.uniprot.org/citations/10862102http://purl.uniprot.org/core/author"Tei C."xsd:string
http://purl.uniprot.org/citations/10862102http://purl.uniprot.org/core/author"Tei C."xsd:string
http://purl.uniprot.org/citations/10862102http://purl.uniprot.org/core/author"Anan R."xsd:string
http://purl.uniprot.org/citations/10862102http://purl.uniprot.org/core/author"Anan R."xsd:string
http://purl.uniprot.org/citations/10862102http://purl.uniprot.org/core/author"Shono H."xsd:string
http://purl.uniprot.org/citations/10862102http://purl.uniprot.org/core/author"Shono H."xsd:string
http://purl.uniprot.org/citations/10862102http://purl.uniprot.org/core/date"2000"xsd:gYear
http://purl.uniprot.org/citations/10862102http://purl.uniprot.org/core/date"2000"xsd:gYear
http://purl.uniprot.org/citations/10862102http://purl.uniprot.org/core/name"Hum. Mutat."xsd:string
http://purl.uniprot.org/citations/10862102http://purl.uniprot.org/core/name"Hum. Mutat."xsd:string
http://purl.uniprot.org/citations/10862102http://purl.uniprot.org/core/pages"584"xsd:string
http://purl.uniprot.org/citations/10862102http://purl.uniprot.org/core/pages"584"xsd:string
http://purl.uniprot.org/citations/10862102http://purl.uniprot.org/core/title"Novel cardiac beta-myosin heavy chain gene missense mutations (R869C and R870C) that cause familial hypertrophic cardiomyopathy."xsd:string
http://purl.uniprot.org/citations/10862102http://purl.uniprot.org/core/title"Novel cardiac beta-myosin heavy chain gene missense mutations (R869C and R870C) that cause familial hypertrophic cardiomyopathy."xsd:string
http://purl.uniprot.org/citations/10862102http://purl.uniprot.org/core/volume"15"xsd:string
http://purl.uniprot.org/citations/10862102http://purl.uniprot.org/core/volume"15"xsd:string
http://purl.uniprot.org/citations/10862102http://www.w3.org/2004/02/skos/core#exactMatchhttp://purl.uniprot.org/pubmed/10862102
http://purl.uniprot.org/citations/10862102http://www.w3.org/2004/02/skos/core#exactMatchhttp://purl.uniprot.org/pubmed/10862102
http://purl.uniprot.org/citations/10862102http://xmlns.com/foaf/0.1/primaryTopicOfhttps://pubmed.ncbi.nlm.nih.gov/10862102
http://purl.uniprot.org/citations/10862102http://xmlns.com/foaf/0.1/primaryTopicOfhttps://pubmed.ncbi.nlm.nih.gov/10862102
http://purl.uniprot.org/uniprot/P12883http://purl.uniprot.org/core/citationhttp://purl.uniprot.org/citations/10862102