@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:NP932382.RAuuFQViidq9KidFI5hMB5uan1vQj16FrXCE0hS7Xm23I130_head { this: np:hasAssertion dgn-np:NP932382.RAuuFQViidq9KidFI5hMB5uan1vQj16FrXCE0hS7Xm23I130_assertion; np:hasProvenance dgn-np:NP932382.RAuuFQViidq9KidFI5hMB5uan1vQj16FrXCE0hS7Xm23I130_provenance; np:hasPublicationInfo dgn-np:NP932382.RAuuFQViidq9KidFI5hMB5uan1vQj16FrXCE0hS7Xm23I130_publicationInfo; a np:Nanopublication . dgn-np:NP932382.RAuuFQViidq9KidFI5hMB5uan1vQj16FrXCE0hS7Xm23I130_assertion a np:Assertion . dgn-np:NP932382.RAuuFQViidq9KidFI5hMB5uan1vQj16FrXCE0hS7Xm23I130_provenance a np:Provenance . dgn-np:NP932382.RAuuFQViidq9KidFI5hMB5uan1vQj16FrXCE0hS7Xm23I130_publicationInfo a np:PublicationInfo . } dgn-np:NP932382.RAuuFQViidq9KidFI5hMB5uan1vQj16FrXCE0hS7Xm23I130_assertion { miriam-gene:2625 a ncit:C16612 . lld:C0018213 a ncit:C7057 . dgn-gda:DGNcf23705d37c474dca9b8a98202db4190 sio:SIO_000628 miriam-gene:2625, lld:C0018213; a sio:SIO_001122 . } dgn-np:NP932382.RAuuFQViidq9KidFI5hMB5uan1vQj16FrXCE0hS7Xm23I130_provenance { dgn-np:NP932382.RAuuFQViidq9KidFI5hMB5uan1vQj16FrXCE0hS7Xm23I130_assertion dcterms:description "[We genotyped -1514T/C (rs17250932) and -1993T/C (rs4794067) polymorphisms of TBX21, - 742C/G polymorphism (rs2184658) of HLX and -1420G/A polymorphism (rs1269486) of GATA3 in genomic DNA samples from Japanese patients; 51 patients with severe Hashimoto's disease (HD), 39 with mild HD, 66 with intractable Graves' disease (GD), in whom remission was difficult to induce, 47 with GD in remission and 79 healthy volunteers.]. 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:22014209; 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:NP932382.RAuuFQViidq9KidFI5hMB5uan1vQj16FrXCE0hS7Xm23I130_publicationInfo { this: dcterms:created "2016-05-13T12:48:47+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" . }