@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:NP891892.RAfEdJ_tjvtc2cJ7ktS9-oRjC2iusozTVWnkQoT19nOFQ130_head { this: np:hasAssertion dgn-np:NP891892.RAfEdJ_tjvtc2cJ7ktS9-oRjC2iusozTVWnkQoT19nOFQ130_assertion; np:hasProvenance dgn-np:NP891892.RAfEdJ_tjvtc2cJ7ktS9-oRjC2iusozTVWnkQoT19nOFQ130_provenance; np:hasPublicationInfo dgn-np:NP891892.RAfEdJ_tjvtc2cJ7ktS9-oRjC2iusozTVWnkQoT19nOFQ130_publicationInfo; a np:Nanopublication . dgn-np:NP891892.RAfEdJ_tjvtc2cJ7ktS9-oRjC2iusozTVWnkQoT19nOFQ130_assertion a np:Assertion . dgn-np:NP891892.RAfEdJ_tjvtc2cJ7ktS9-oRjC2iusozTVWnkQoT19nOFQ130_provenance a np:Provenance . dgn-np:NP891892.RAfEdJ_tjvtc2cJ7ktS9-oRjC2iusozTVWnkQoT19nOFQ130_publicationInfo a np:PublicationInfo . } dgn-np:NP891892.RAfEdJ_tjvtc2cJ7ktS9-oRjC2iusozTVWnkQoT19nOFQ130_assertion { miriam-gene:28955 a ncit:C16612 . lld:C0011854 a ncit:C7057 . dgn-gda:DGN7376368f4d20be6b42f61b2a2ff0b62d sio:SIO_000628 miriam-gene:28955, lld:C0011854; a sio:SIO_001121 . } dgn-np:NP891892.RAfEdJ_tjvtc2cJ7ktS9-oRjC2iusozTVWnkQoT19nOFQ130_provenance { dgn-np:NP891892.RAfEdJ_tjvtc2cJ7ktS9-oRjC2iusozTVWnkQoT19nOFQ130_assertion dcterms:description "[In reciprocal experiments, a 20 kb fragment of intron 19 of CLEC16A, containing SNPs associated with T1D and MS, as well as with DEXI expression, interacted with the promotor region of DEXI but not with candidate DNA fragments containing other potential causal genes in the region, including CLEC16A.]. 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:21989056; prov:wasDerivedFrom dgn-void:befree-20150227; prov:wasGeneratedBy eco:ECO_0000203 . dgn-void:befree-20150227 pav:importedOn "2015-02-27"^^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:NP891892.RAfEdJ_tjvtc2cJ7ktS9-oRjC2iusozTVWnkQoT19nOFQ130_publicationInfo { this: dcterms:created "2015-08-25T14:46:44+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 "v3.0.0.0" . dgn-void:disgenetv3.0rdf pav:version "v3.0.0" . }