@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:NP1267862.RAGI6QbIIlULxf9nI5scEL8clHy39LzQXPwdcYEV1vMcI130_head { this: np:hasAssertion dgn-np:NP1267862.RAGI6QbIIlULxf9nI5scEL8clHy39LzQXPwdcYEV1vMcI130_assertion; np:hasProvenance dgn-np:NP1267862.RAGI6QbIIlULxf9nI5scEL8clHy39LzQXPwdcYEV1vMcI130_provenance; np:hasPublicationInfo dgn-np:NP1267862.RAGI6QbIIlULxf9nI5scEL8clHy39LzQXPwdcYEV1vMcI130_publicationInfo; a np:Nanopublication . dgn-np:NP1267862.RAGI6QbIIlULxf9nI5scEL8clHy39LzQXPwdcYEV1vMcI130_assertion a np:Assertion . dgn-np:NP1267862.RAGI6QbIIlULxf9nI5scEL8clHy39LzQXPwdcYEV1vMcI130_provenance a np:Provenance . dgn-np:NP1267862.RAGI6QbIIlULxf9nI5scEL8clHy39LzQXPwdcYEV1vMcI130_publicationInfo a np:PublicationInfo . } dgn-np:NP1267862.RAGI6QbIIlULxf9nI5scEL8clHy39LzQXPwdcYEV1vMcI130_assertion { miriam-gene:6261 a ncit:C16612 . lld:C0024591 a ncit:C7057 . dgn-gda:DGN1b7ac99c99a13f5998970a7df75bf8c8 sio:SIO_000628 miriam-gene:6261, lld:C0024591; a sio:SIO_001121 . } dgn-np:NP1267862.RAGI6QbIIlULxf9nI5scEL8clHy39LzQXPwdcYEV1vMcI130_provenance { dgn-np:NP1267862.RAGI6QbIIlULxf9nI5scEL8clHy39LzQXPwdcYEV1vMcI130_assertion dcterms:description "[Sixty-two MH susceptible individuals presenting to the same diagnostic centre had copy deoxyribonucleic acid, derived from muscle ribonucleic acid, sequenced to identify variants with the potential to be responsible for the MH phenotype in both RYR1 and CACNA1S.]. 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:25735680; 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:NP1267862.RAGI6QbIIlULxf9nI5scEL8clHy39LzQXPwdcYEV1vMcI130_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" . }