@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:NP90280.RAeKijOGCc1EZ_FboN3W79NpAroX_Tcy0rHuE3QXS43Gk130_head { this: np:hasAssertion dgn-np:NP90280.RAeKijOGCc1EZ_FboN3W79NpAroX_Tcy0rHuE3QXS43Gk130_assertion; np:hasProvenance dgn-np:NP90280.RAeKijOGCc1EZ_FboN3W79NpAroX_Tcy0rHuE3QXS43Gk130_provenance; np:hasPublicationInfo dgn-np:NP90280.RAeKijOGCc1EZ_FboN3W79NpAroX_Tcy0rHuE3QXS43Gk130_publicationInfo; a np:Nanopublication . dgn-np:NP90280.RAeKijOGCc1EZ_FboN3W79NpAroX_Tcy0rHuE3QXS43Gk130_assertion a np:Assertion . dgn-np:NP90280.RAeKijOGCc1EZ_FboN3W79NpAroX_Tcy0rHuE3QXS43Gk130_provenance a np:Provenance . dgn-np:NP90280.RAeKijOGCc1EZ_FboN3W79NpAroX_Tcy0rHuE3QXS43Gk130_publicationInfo a np:PublicationInfo . } dgn-np:NP90280.RAeKijOGCc1EZ_FboN3W79NpAroX_Tcy0rHuE3QXS43Gk130_assertion { miriam-gene:4607 a ncit:C16612 . lld:C0878544 a ncit:C7057 . dgn-gda:DGN0044e637ef92eb37986d975f3c652030 sio:SIO_000628 miriam-gene:4607, lld:C0878544; a sio:SIO_001122 . } dgn-np:NP90280.RAeKijOGCc1EZ_FboN3W79NpAroX_Tcy0rHuE3QXS43Gk130_provenance { dgn-np:NP90280.RAeKijOGCc1EZ_FboN3W79NpAroX_Tcy0rHuE3QXS43Gk130_assertion dcterms:description "[ Although cases of adult patients with DCM caused by mutations of the genes encoding sarcomeric or cytoskeletal proteins of cardiomyocytes are infrequent in Japan, it may be advisable to screen older DCM patients for MYBPC3 mutations, and male patients wi]. 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:15671604; prov:wasDerivedFrom dgn-void:gad-20150221; prov:wasGeneratedBy eco:ECO_0000203 . dgn-void:gad-20150221 pav:importedOn "2015-02-21"^^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:NP90280.RAeKijOGCc1EZ_FboN3W79NpAroX_Tcy0rHuE3QXS43Gk130_publicationInfo { this: dcterms:created "2016-05-13T12:42:29+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" . }