@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:NP1126449.RAuBNJKJ6uZipW85hBkiM74MnBFCFF_in6YpBoa7ERd-o130_head { this: np:hasAssertion dgn-np:NP1126449.RAuBNJKJ6uZipW85hBkiM74MnBFCFF_in6YpBoa7ERd-o130_assertion; np:hasProvenance dgn-np:NP1126449.RAuBNJKJ6uZipW85hBkiM74MnBFCFF_in6YpBoa7ERd-o130_provenance; np:hasPublicationInfo dgn-np:NP1126449.RAuBNJKJ6uZipW85hBkiM74MnBFCFF_in6YpBoa7ERd-o130_publicationInfo; a np:Nanopublication . dgn-np:NP1126449.RAuBNJKJ6uZipW85hBkiM74MnBFCFF_in6YpBoa7ERd-o130_assertion a np:Assertion . dgn-np:NP1126449.RAuBNJKJ6uZipW85hBkiM74MnBFCFF_in6YpBoa7ERd-o130_provenance a np:Provenance . dgn-np:NP1126449.RAuBNJKJ6uZipW85hBkiM74MnBFCFF_in6YpBoa7ERd-o130_publicationInfo a np:PublicationInfo . } dgn-np:NP1126449.RAuBNJKJ6uZipW85hBkiM74MnBFCFF_in6YpBoa7ERd-o130_assertion { miriam-gene:8989 a ncit:C16612 . lld:C0391976 a ncit:C7057 . dgn-gda:DGN30edd14f3731db1866d854d388bc39ce sio:SIO_000628 miriam-gene:8989, lld:C0391976; a sio:SIO_001121 . } dgn-np:NP1126449.RAuBNJKJ6uZipW85hBkiM74MnBFCFF_in6YpBoa7ERd-o130_provenance { dgn-np:NP1126449.RAuBNJKJ6uZipW85hBkiM74MnBFCFF_in6YpBoa7ERd-o130_assertion dcterms:description "[We performed a genome-wide linkage scan with microsatellite markers after excluding mutations in three known genes (SCN9A, SCN10A, and TRPA1) that cause similar pain syndrome to our findings, and we mapped the genetic locus to a 7.81 Mb region on chromosome 3p22.3-p21.32.]. 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:24207120; 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:NP1126449.RAuBNJKJ6uZipW85hBkiM74MnBFCFF_in6YpBoa7ERd-o130_publicationInfo { this: dcterms:created "2016-05-13T12:50:17+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" . }