@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:NP419414.RAlFU4lrpKeYZTGMlXI5ZfXRfuuSr9vlnZXsPcJjhnzFY130_head { this: np:hasAssertion dgn-np:NP419414.RAlFU4lrpKeYZTGMlXI5ZfXRfuuSr9vlnZXsPcJjhnzFY130_assertion; np:hasProvenance dgn-np:NP419414.RAlFU4lrpKeYZTGMlXI5ZfXRfuuSr9vlnZXsPcJjhnzFY130_provenance; np:hasPublicationInfo dgn-np:NP419414.RAlFU4lrpKeYZTGMlXI5ZfXRfuuSr9vlnZXsPcJjhnzFY130_publicationInfo; a np:Nanopublication . dgn-np:NP419414.RAlFU4lrpKeYZTGMlXI5ZfXRfuuSr9vlnZXsPcJjhnzFY130_assertion a np:Assertion . dgn-np:NP419414.RAlFU4lrpKeYZTGMlXI5ZfXRfuuSr9vlnZXsPcJjhnzFY130_provenance a np:Provenance . dgn-np:NP419414.RAlFU4lrpKeYZTGMlXI5ZfXRfuuSr9vlnZXsPcJjhnzFY130_publicationInfo a np:PublicationInfo . } dgn-np:NP419414.RAlFU4lrpKeYZTGMlXI5ZfXRfuuSr9vlnZXsPcJjhnzFY130_assertion { miriam-gene:2626 a ncit:C16612 . lld:C0007193 a ncit:C7057 . dgn-gda:DGNce410ee80279b921864e257c819575ef sio:SIO_000628 miriam-gene:2626, lld:C0007193; a sio:SIO_001121 . } dgn-np:NP419414.RAlFU4lrpKeYZTGMlXI5ZfXRfuuSr9vlnZXsPcJjhnzFY130_provenance { dgn-np:NP419414.RAlFU4lrpKeYZTGMlXI5ZfXRfuuSr9vlnZXsPcJjhnzFY130_assertion dcterms:description "[The findings expand the mutational spectrum of GATA4 linked to DCM and provide novel insight into the molecular etiology involved in DCM, suggesting the potential implications in the early prophylaxis and allele-specific treatment for this common type of cardiomyopathy.]. 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:24366163; prov:wasDerivedFrom dgn-void:befree-20150227; prov:wasGeneratedBy eco:ECO_0000203 . dgn-void:befree-20150227 pav:importedOn "2015-02-27"^^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:NP419414.RAlFU4lrpKeYZTGMlXI5ZfXRfuuSr9vlnZXsPcJjhnzFY130_publicationInfo { this: dcterms:created "2015-08-25T14:41:44+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 "v3.0.0.0" . dgn-void:disgenetv3.0rdf pav:version "v3.0.0" . }