@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:NP757136.RAxUQ30VMR-EqclGgXFTdSaTpV2eEdx1Rs06rUEO7Eygo130_head { this: np:hasAssertion dgn-np:NP757136.RAxUQ30VMR-EqclGgXFTdSaTpV2eEdx1Rs06rUEO7Eygo130_assertion; np:hasProvenance dgn-np:NP757136.RAxUQ30VMR-EqclGgXFTdSaTpV2eEdx1Rs06rUEO7Eygo130_provenance; np:hasPublicationInfo dgn-np:NP757136.RAxUQ30VMR-EqclGgXFTdSaTpV2eEdx1Rs06rUEO7Eygo130_publicationInfo; a np:Nanopublication . dgn-np:NP757136.RAxUQ30VMR-EqclGgXFTdSaTpV2eEdx1Rs06rUEO7Eygo130_assertion a np:Assertion . dgn-np:NP757136.RAxUQ30VMR-EqclGgXFTdSaTpV2eEdx1Rs06rUEO7Eygo130_provenance a np:Provenance . dgn-np:NP757136.RAxUQ30VMR-EqclGgXFTdSaTpV2eEdx1Rs06rUEO7Eygo130_publicationInfo a np:PublicationInfo . } dgn-np:NP757136.RAxUQ30VMR-EqclGgXFTdSaTpV2eEdx1Rs06rUEO7Eygo130_assertion { miriam-gene:6323 a ncit:C16612 . lld:C0014544 a ncit:C7057 . dgn-gda:DGN96a7ece4c5be8109dc91748808952e7b sio:SIO_000628 miriam-gene:6323, lld:C0014544; a sio:SIO_001121 . } dgn-np:NP757136.RAxUQ30VMR-EqclGgXFTdSaTpV2eEdx1Rs06rUEO7Eygo130_provenance { dgn-np:NP757136.RAxUQ30VMR-EqclGgXFTdSaTpV2eEdx1Rs06rUEO7Eygo130_assertion dcterms:description "[Furthermore, whether the migraine of the mother could be influenced by her SCN1A mutation mosaicism is not known, but increased awareness of migraine in future studies of SCN1A related epilepsies could clarify this intriguing link between migraine and epilepsy.]. 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:19673951; 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:NP757136.RAxUQ30VMR-EqclGgXFTdSaTpV2eEdx1Rs06rUEO7Eygo130_publicationInfo { this: dcterms:created "2016-05-13T12:47:28+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" . }