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SubjectPredicateObject
http://purl.uniprot.org/citations/9272156http://xmlns.com/foaf/0.1/primaryTopicOfhttps://pubmed.ncbi.nlm.nih.gov/9272156
http://purl.uniprot.org/citations/9272156http://purl.uniprot.org/core/author"Wang Y."xsd:string
http://purl.uniprot.org/citations/9272156http://purl.uniprot.org/core/author"Friedl W."xsd:string
http://purl.uniprot.org/citations/9272156http://purl.org/dc/terms/identifier"doi:10.1007/s004390050517"xsd:string
http://purl.uniprot.org/citations/9272156http://purl.uniprot.org/core/date"1997"xsd:gYear
http://purl.uniprot.org/citations/9272156http://purl.uniprot.org/core/author"Lamberti C."xsd:string
http://purl.uniprot.org/uniprot/P40692http://purl.uniprot.org/core/citationhttp://purl.uniprot.org/citations/9272156
http://purl.uniprot.org/citations/9272156http://purl.uniprot.org/core/author"Propping P."xsd:string
http://purl.uniprot.org/citations/9272156http://www.w3.org/1999/02/22-rdf-syntax-ns#typehttp://purl.uniprot.org/core/Journal_Citation
http://purl.uniprot.org/citations/9272156http://purl.uniprot.org/core/pages"362-364"xsd:string
http://purl.uniprot.org/uniprot/#_P40692-citation-9272156http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/9272156
http://purl.uniprot.org/uniprot/P40692#attribution-959EFCBCCA6B0A92483B3F1DAD00FFAChttp://purl.uniprot.org/core/sourcehttp://purl.uniprot.org/citations/9272156
http://purl.uniprot.org/citations/9272156http://purl.uniprot.org/core/volume"100"xsd:string
http://purl.uniprot.org/citations/9272156http://purl.uniprot.org/core/author"Kruse R."xsd:string
http://purl.uniprot.org/citations/9272156http://purl.uniprot.org/core/name"Hum. Genet."xsd:string
http://purl.uniprot.org/citations/9272156http://www.w3.org/2004/02/skos/core#exactMatchhttp://purl.uniprot.org/pubmed/9272156
http://purl.uniprot.org/citations/9272156http://purl.uniprot.org/core/author"Ruelfs C."xsd:string
http://purl.uniprot.org/citations/9272156http://purl.uniprot.org/core/title"Hereditary nonpolyposis colorectal cancer: causative role of a germline missense mutation in the hMLH1 gene confirmed by the independent occurrence of the same somatic mutation in tumour tissue."xsd:string