@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:NP84331.RA4imde5k6GtqlgBaqY8TcE8X8WmlyIoiRYSGHXV3LC44130_head { this: np:hasAssertion dgn-np:NP84331.RA4imde5k6GtqlgBaqY8TcE8X8WmlyIoiRYSGHXV3LC44130_assertion; np:hasProvenance dgn-np:NP84331.RA4imde5k6GtqlgBaqY8TcE8X8WmlyIoiRYSGHXV3LC44130_provenance; np:hasPublicationInfo dgn-np:NP84331.RA4imde5k6GtqlgBaqY8TcE8X8WmlyIoiRYSGHXV3LC44130_publicationInfo; a np:Nanopublication . dgn-np:NP84331.RA4imde5k6GtqlgBaqY8TcE8X8WmlyIoiRYSGHXV3LC44130_assertion a np:Assertion . dgn-np:NP84331.RA4imde5k6GtqlgBaqY8TcE8X8WmlyIoiRYSGHXV3LC44130_provenance a np:Provenance . dgn-np:NP84331.RA4imde5k6GtqlgBaqY8TcE8X8WmlyIoiRYSGHXV3LC44130_publicationInfo a np:PublicationInfo . } dgn-np:NP84331.RA4imde5k6GtqlgBaqY8TcE8X8WmlyIoiRYSGHXV3LC44130_assertion { miriam-gene:4282 a ncit:C16612 . lld:C0003873 a ncit:C7057 . dgn-gda:DGNaf994b16ec190a26f73dd523a4913069 sio:SIO_000628 miriam-gene:4282, lld:C0003873; a sio:SIO_001122 . } dgn-np:NP84331.RA4imde5k6GtqlgBaqY8TcE8X8WmlyIoiRYSGHXV3LC44130_provenance { dgn-np:NP84331.RA4imde5k6GtqlgBaqY8TcE8X8WmlyIoiRYSGHXV3LC44130_assertion dcterms:description "[Up to 200 unrelated German RA and JRA patients each and 300-400 healthy controls have been genotyped for HLA-DRB1, TNFa, TNFA -238a/g, TNFA -308a/g, TNFA -857c/t, TNFR1 -609g/t, TNFR1 P12P, TNFR2 del 15bp, IKBL -332a/g, IKBL -132t/a, IKBL C224R, CTLA4 -318c/t, CTLA4 T17A, PTPRC P57P, MIF -173g/c, the MIF and IFNG microsatellites as well as for D17S795, D17S807, D17S1821 by polyacrylamide gel electrophoresis, single-strand conformation polymorphism analysis, restriction fragment length polymorphism analysis or allele specific hybridization.]. 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:15018649; 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:NP84331.RA4imde5k6GtqlgBaqY8TcE8X8WmlyIoiRYSGHXV3LC44130_publicationInfo { this: dcterms:created "2016-05-13T12:42:26+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" . }