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http://purl.uniprot.org/SHA-384/B4979F29B8D21EF6C5E9114077483EB8D22378F8E01B19121A85A6FFA554F0145F13C3CFDA5AAF483F0BC0E4BA4DFC3Ehttp://www.w3.org/1999/02/22-rdf-syntax-ns#typehttp://purl.uniprot.org/core/Annotation
http://purl.uniprot.org/SHA-384/B4979F29B8D21EF6C5E9114077483EB8D22378F8E01B19121A85A6FFA554F0145F13C3CFDA5AAF483F0BC0E4BA4DFC3Ehttp://www.w3.org/2000/01/rdf-schema#comment"We found a remarkable genetic heterogeneity in the studied families with USH1 with a variety of mutations among which three were novel. These novel mutations will be included in the NADf mutation screening chip that will allow a higher diagnosis efficiency of this extremely genetically heterogeneous disease."xsd:string
http://purl.uniprot.org/uniprot/#_5417B5ED6D4C97AB19772FB59F51A6F89FF32A17995DCC21B3374C55429DDC24383A55170ABDE5B3ADAE88E361BF1D17http://www.w3.org/1999/02/22-rdf-syntax-ns#subjecthttp://purl.uniprot.org/SHA-384/B4979F29B8D21EF6C5E9114077483EB8D22378F8E01B19121A85A6FFA554F0145F13C3CFDA5AAF483F0BC0E4BA4DFC3E
http://purl.uniprot.org/uniprot/A0A087WTR6http://purl.uniprot.org/core/mappedAnnotationhttp://purl.uniprot.org/SHA-384/B4979F29B8D21EF6C5E9114077483EB8D22378F8E01B19121A85A6FFA554F0145F13C3CFDA5AAF483F0BC0E4BA4DFC3E
http://purl.uniprot.org/uniprot/#_A0A087WTR6-mappedCitation-27440999http://purl.uniprot.org/core/mappedAnnotationhttp://purl.uniprot.org/SHA-384/B4979F29B8D21EF6C5E9114077483EB8D22378F8E01B19121A85A6FFA554F0145F13C3CFDA5AAF483F0BC0E4BA4DFC3E