@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:NP851767.RAahevMAJGe6WIbnxreqM8wn8gNsb7sEpMdeIHYyR_JTg130_head { this: np:hasAssertion dgn-np:NP851767.RAahevMAJGe6WIbnxreqM8wn8gNsb7sEpMdeIHYyR_JTg130_assertion; np:hasProvenance dgn-np:NP851767.RAahevMAJGe6WIbnxreqM8wn8gNsb7sEpMdeIHYyR_JTg130_provenance; np:hasPublicationInfo dgn-np:NP851767.RAahevMAJGe6WIbnxreqM8wn8gNsb7sEpMdeIHYyR_JTg130_publicationInfo; a np:Nanopublication . dgn-np:NP851767.RAahevMAJGe6WIbnxreqM8wn8gNsb7sEpMdeIHYyR_JTg130_assertion a np:Assertion . dgn-np:NP851767.RAahevMAJGe6WIbnxreqM8wn8gNsb7sEpMdeIHYyR_JTg130_provenance a np:Provenance . dgn-np:NP851767.RAahevMAJGe6WIbnxreqM8wn8gNsb7sEpMdeIHYyR_JTg130_publicationInfo a np:PublicationInfo . } dgn-np:NP851767.RAahevMAJGe6WIbnxreqM8wn8gNsb7sEpMdeIHYyR_JTg130_assertion { miriam-gene:6901 a ncit:C16612 . lld:C0574083 a ncit:C7057 . dgn-gda:DGNb22ab4b0d450567e478ff07d47638ab6 sio:SIO_000628 miriam-gene:6901, lld:C0574083; a sio:SIO_001121 . } dgn-np:NP851767.RAahevMAJGe6WIbnxreqM8wn8gNsb7sEpMdeIHYyR_JTg130_provenance { dgn-np:NP851767.RAahevMAJGe6WIbnxreqM8wn8gNsb7sEpMdeIHYyR_JTg130_assertion dcterms:description "[Tafazzin knockdown mice provide the first mammalian model system for Barth syndrome in which the pathophysiological relationships between altered content of mitochondrial phospholipids, ultrastructural abnormalities, myocardial and mitochondrial dysfunction, and clinical outcome can be completely investigated.]. 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:21068380; 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:NP851767.RAahevMAJGe6WIbnxreqM8wn8gNsb7sEpMdeIHYyR_JTg130_publicationInfo { this: dcterms:created "2016-05-13T12:48:10+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" . }