@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:NP1266997.RAel8s5lyyyDTXkMAYlktCyislfOtVauZrgqjMGofHZMo130_head { this: np:hasAssertion dgn-np:NP1266997.RAel8s5lyyyDTXkMAYlktCyislfOtVauZrgqjMGofHZMo130_assertion; np:hasProvenance dgn-np:NP1266997.RAel8s5lyyyDTXkMAYlktCyislfOtVauZrgqjMGofHZMo130_provenance; np:hasPublicationInfo dgn-np:NP1266997.RAel8s5lyyyDTXkMAYlktCyislfOtVauZrgqjMGofHZMo130_publicationInfo; a np:Nanopublication . dgn-np:NP1266997.RAel8s5lyyyDTXkMAYlktCyislfOtVauZrgqjMGofHZMo130_assertion a np:Assertion . dgn-np:NP1266997.RAel8s5lyyyDTXkMAYlktCyislfOtVauZrgqjMGofHZMo130_provenance a np:Provenance . dgn-np:NP1266997.RAel8s5lyyyDTXkMAYlktCyislfOtVauZrgqjMGofHZMo130_publicationInfo a np:PublicationInfo . } dgn-np:NP1266997.RAel8s5lyyyDTXkMAYlktCyislfOtVauZrgqjMGofHZMo130_assertion { miriam-gene:6910 a ncit:C16612 . lld:C0007193 a ncit:C7057 . dgn-gda:DGN2ff54c59d3f3520e8aefda49e804ac6d sio:SIO_000628 miriam-gene:6910, lld:C0007193; a sio:SIO_001121 . } dgn-np:NP1266997.RAel8s5lyyyDTXkMAYlktCyislfOtVauZrgqjMGofHZMo130_provenance { dgn-np:NP1266997.RAel8s5lyyyDTXkMAYlktCyislfOtVauZrgqjMGofHZMo130_assertion dcterms:description "[This study firstly associates TBX5 loss-of-function mutation with enhanced susceptibility to DCM, providing novel insight into the molecular mechanisms of DCM, and suggesting the potential implications in the development of new treatment strategies for this common form of myocardial disorder.]. 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:25725155; 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:NP1266997.RAel8s5lyyyDTXkMAYlktCyislfOtVauZrgqjMGofHZMo130_publicationInfo { this: dcterms:created "2016-05-13T12:51:20+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" . }