@prefix this: . @prefix rdfs: . @prefix xsd: . @prefix sio: . @prefix ncit: . @prefix lld: . @prefix miriam-gene: . @prefix miriam-pubmed: . @prefix eco: . @prefix wi: . @prefix prov: . @prefix pav: . @prefix prv: . @prefix dcterms: . @prefix np: . @prefix dgn-np: . @prefix dgn-gda: . @prefix dgn-void: . dgn-np:NP1053102.RA4iTKMLND6Y_iMtEhLsPxOpVQP8I5T-Z4iHq1EqM4cjc130_head { this: np:hasAssertion dgn-np:NP1053102.RA4iTKMLND6Y_iMtEhLsPxOpVQP8I5T-Z4iHq1EqM4cjc130_assertion; np:hasProvenance dgn-np:NP1053102.RA4iTKMLND6Y_iMtEhLsPxOpVQP8I5T-Z4iHq1EqM4cjc130_provenance; np:hasPublicationInfo dgn-np:NP1053102.RA4iTKMLND6Y_iMtEhLsPxOpVQP8I5T-Z4iHq1EqM4cjc130_publicationInfo; a np:Nanopublication . dgn-np:NP1053102.RA4iTKMLND6Y_iMtEhLsPxOpVQP8I5T-Z4iHq1EqM4cjc130_assertion a np:Assertion . dgn-np:NP1053102.RA4iTKMLND6Y_iMtEhLsPxOpVQP8I5T-Z4iHq1EqM4cjc130_provenance a np:Provenance . dgn-np:NP1053102.RA4iTKMLND6Y_iMtEhLsPxOpVQP8I5T-Z4iHq1EqM4cjc130_publicationInfo a np:PublicationInfo . } dgn-np:NP1053102.RA4iTKMLND6Y_iMtEhLsPxOpVQP8I5T-Z4iHq1EqM4cjc130_assertion { miriam-gene:25937 a ncit:C16612 . lld:C0574083 a ncit:C7057 . dgn-gda:DGN5ee12e34e366c3ec857041892d359c56 sio:SIO_000628 miriam-gene:25937, lld:C0574083; a sio:SIO_001122 . } dgn-np:NP1053102.RA4iTKMLND6Y_iMtEhLsPxOpVQP8I5T-Z4iHq1EqM4cjc130_provenance { dgn-np:NP1053102.RA4iTKMLND6Y_iMtEhLsPxOpVQP8I5T-Z4iHq1EqM4cjc130_assertion dcterms:description "[We confirmed the diagnosis of BS with sequence analysis of the TAZ gene, and found five new mutations, c.641A>G p.His214Arg, c.284dupG (p.Thr96Aspfs*37), c.678_691del14 (p.Tyr227Trpfs*79), g.8009_16445del8437 and g.[9777_9814del38; 9911-?_14402del] and the known nonsense mutation c.367C>T (p.Arg123Term).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en; wi:evidence dgn-void:source_evidence_literature; sio:SIO_000772 miriam-pubmed:23409742; prov:wasDerivedFrom dgn-void:befree-2016; prov:wasGeneratedBy eco:ECO_0000203 . dgn-void:befree-2016 pav:importedOn "2016-02-19"^^xsd:date . dgn-void:source_evidence_literature a eco:ECO_0000212; rdfs:comment "Gene-disease associations inferred from text-mining the literature."@en; rdfs:label "DisGeNET evidence - LITERATURE"@en . } dgn-np:NP1053102.RA4iTKMLND6Y_iMtEhLsPxOpVQP8I5T-Z4iHq1EqM4cjc130_publicationInfo { this: dcterms:created "2016-05-13T12:49:43+02:00"^^xsd:dateTime; dcterms:rights ; dcterms:rightsHolder dgn-void:IBIGroup; dcterms:subject sio:SIO_000983; prv:usedData dgn-void:disgenetv3.0rdf; pav:authoredBy , , , , ; pav:createdBy ; pav:version "v4.0.0.0" . dgn-void:disgenetv3.0rdf pav:version "v4.0.0" . }