@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:NP1256498.RA9iLWi6IWVmVarlpNh-rLX7vxU7eUe1JJ3QUwM0VVHK4130_head { this: np:hasAssertion dgn-np:NP1256498.RA9iLWi6IWVmVarlpNh-rLX7vxU7eUe1JJ3QUwM0VVHK4130_assertion; np:hasProvenance dgn-np:NP1256498.RA9iLWi6IWVmVarlpNh-rLX7vxU7eUe1JJ3QUwM0VVHK4130_provenance; np:hasPublicationInfo dgn-np:NP1256498.RA9iLWi6IWVmVarlpNh-rLX7vxU7eUe1JJ3QUwM0VVHK4130_publicationInfo; a np:Nanopublication . dgn-np:NP1256498.RA9iLWi6IWVmVarlpNh-rLX7vxU7eUe1JJ3QUwM0VVHK4130_assertion a np:Assertion . dgn-np:NP1256498.RA9iLWi6IWVmVarlpNh-rLX7vxU7eUe1JJ3QUwM0VVHK4130_provenance a np:Provenance . dgn-np:NP1256498.RA9iLWi6IWVmVarlpNh-rLX7vxU7eUe1JJ3QUwM0VVHK4130_publicationInfo a np:PublicationInfo . } dgn-np:NP1256498.RA9iLWi6IWVmVarlpNh-rLX7vxU7eUe1JJ3QUwM0VVHK4130_assertion { miriam-gene:1312 a ncit:C16612 . lld:C0338480 a ncit:C7057 . dgn-gda:DGN9dec9c905115336af1f3087fac23b572 sio:SIO_000628 miriam-gene:1312, lld:C0338480; a sio:SIO_001121 . } dgn-np:NP1256498.RA9iLWi6IWVmVarlpNh-rLX7vxU7eUe1JJ3QUwM0VVHK4130_provenance { dgn-np:NP1256498.RA9iLWi6IWVmVarlpNh-rLX7vxU7eUe1JJ3QUwM0VVHK4130_assertion dcterms:description "[Using T1-weighted and resting functional MRI, we evaluated the effect of COMT genetic variations on migraine and possible interactions between COMT and the disease in brain structure and function in 135 females with migraine without aura (MWoA) and 111 matched health controls (HC).]. 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:25598522; 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:NP1256498.RA9iLWi6IWVmVarlpNh-rLX7vxU7eUe1JJ3QUwM0VVHK4130_publicationInfo { this: dcterms:created "2016-05-13T12:51:15+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" . }