@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:NP68382.RANRCVKYu0wuWff-yh12acGFD8RM4jT3TEn7SHgz_bvIM130_head { this: np:hasAssertion dgn-np:NP68382.RANRCVKYu0wuWff-yh12acGFD8RM4jT3TEn7SHgz_bvIM130_assertion; np:hasProvenance dgn-np:NP68382.RANRCVKYu0wuWff-yh12acGFD8RM4jT3TEn7SHgz_bvIM130_provenance; np:hasPublicationInfo dgn-np:NP68382.RANRCVKYu0wuWff-yh12acGFD8RM4jT3TEn7SHgz_bvIM130_publicationInfo; a np:Nanopublication . dgn-np:NP68382.RANRCVKYu0wuWff-yh12acGFD8RM4jT3TEn7SHgz_bvIM130_assertion a np:Assertion . dgn-np:NP68382.RANRCVKYu0wuWff-yh12acGFD8RM4jT3TEn7SHgz_bvIM130_provenance a np:Provenance . dgn-np:NP68382.RANRCVKYu0wuWff-yh12acGFD8RM4jT3TEn7SHgz_bvIM130_publicationInfo a np:PublicationInfo . } dgn-np:NP68382.RANRCVKYu0wuWff-yh12acGFD8RM4jT3TEn7SHgz_bvIM130_assertion { miriam-gene:3126 a ncit:C16612 . lld:C0011854 a ncit:C7057 . dgn-gda:DGN4528e65d13b69ce11f799eb3769ee623 sio:SIO_000628 miriam-gene:3126, lld:C0011854; a sio:SIO_001122 . } dgn-np:NP68382.RANRCVKYu0wuWff-yh12acGFD8RM4jT3TEn7SHgz_bvIM130_provenance { dgn-np:NP68382.RANRCVKYu0wuWff-yh12acGFD8RM4jT3TEn7SHgz_bvIM130_assertion dcterms:description "[One DR51-related haplotype DRB1*1502x, DRB5*0102x, DQA1*0101/4, DQB1*0501, would appear to be characteristic of Thai populations, as it was the most common DR2 haplotype in all five study groups and is also prevalent in other mainland southeast Asians, bu]. 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:11082517; prov:wasDerivedFrom dgn-void:gad-20150221; prov:wasGeneratedBy eco:ECO_0000203 . dgn-void:gad-20150221 pav:importedOn "2015-02-21"^^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:NP68382.RANRCVKYu0wuWff-yh12acGFD8RM4jT3TEn7SHgz_bvIM130_publicationInfo { this: dcterms:created "2016-05-13T12:42:19+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" . }