@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:NP588758.RAuX24x0b1RFePqTj1Lgu1tuJlGjsZCReEuniR_AK4OSA130_head { this: np:hasAssertion dgn-np:NP588758.RAuX24x0b1RFePqTj1Lgu1tuJlGjsZCReEuniR_AK4OSA130_assertion; np:hasProvenance dgn-np:NP588758.RAuX24x0b1RFePqTj1Lgu1tuJlGjsZCReEuniR_AK4OSA130_provenance; np:hasPublicationInfo dgn-np:NP588758.RAuX24x0b1RFePqTj1Lgu1tuJlGjsZCReEuniR_AK4OSA130_publicationInfo; a np:Nanopublication . dgn-np:NP588758.RAuX24x0b1RFePqTj1Lgu1tuJlGjsZCReEuniR_AK4OSA130_assertion a np:Assertion . dgn-np:NP588758.RAuX24x0b1RFePqTj1Lgu1tuJlGjsZCReEuniR_AK4OSA130_provenance a np:Provenance . dgn-np:NP588758.RAuX24x0b1RFePqTj1Lgu1tuJlGjsZCReEuniR_AK4OSA130_publicationInfo a np:PublicationInfo . } dgn-np:NP588758.RAuX24x0b1RFePqTj1Lgu1tuJlGjsZCReEuniR_AK4OSA130_assertion { miriam-gene:6262 a ncit:C16612 . lld:C0023976 a ncit:C7057 . dgn-gda:DGNf3445664f26d6fd3c0fcef4bb056e51e sio:SIO_000628 miriam-gene:6262, lld:C0023976; a sio:SIO_001121 . } dgn-np:NP588758.RAuX24x0b1RFePqTj1Lgu1tuJlGjsZCReEuniR_AK4OSA130_provenance { dgn-np:NP588758.RAuX24x0b1RFePqTj1Lgu1tuJlGjsZCReEuniR_AK4OSA130_assertion dcterms:description "[In this cardiac channel-focused molecular autopsy investigation of SUD, over one-third of decedents harbored a putative cardiac channel mutation: 7 previously reported to host mutations in the RyR2-encoded calcium release channel and now 10 with LQTS susceptibility mutations.]. 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:17222736; 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:NP588758.RAuX24x0b1RFePqTj1Lgu1tuJlGjsZCReEuniR_AK4OSA130_publicationInfo { this: dcterms:created "2016-05-13T12:46:12+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" . }