@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:NP1000978.RAp9oRsFfPz2HZ-kGxFj2S5QFPd0mFlV98IHvKj00SCyk130_head { this: np:hasAssertion dgn-np:NP1000978.RAp9oRsFfPz2HZ-kGxFj2S5QFPd0mFlV98IHvKj00SCyk130_assertion; np:hasProvenance dgn-np:NP1000978.RAp9oRsFfPz2HZ-kGxFj2S5QFPd0mFlV98IHvKj00SCyk130_provenance; np:hasPublicationInfo dgn-np:NP1000978.RAp9oRsFfPz2HZ-kGxFj2S5QFPd0mFlV98IHvKj00SCyk130_publicationInfo; a np:Nanopublication . dgn-np:NP1000978.RAp9oRsFfPz2HZ-kGxFj2S5QFPd0mFlV98IHvKj00SCyk130_assertion a np:Assertion . dgn-np:NP1000978.RAp9oRsFfPz2HZ-kGxFj2S5QFPd0mFlV98IHvKj00SCyk130_provenance a np:Provenance . dgn-np:NP1000978.RAp9oRsFfPz2HZ-kGxFj2S5QFPd0mFlV98IHvKj00SCyk130_publicationInfo a np:PublicationInfo . } dgn-np:NP1000978.RAp9oRsFfPz2HZ-kGxFj2S5QFPd0mFlV98IHvKj00SCyk130_assertion { miriam-gene:9447 a ncit:C16612 . lld:C0024141 a ncit:C7057 . dgn-gda:DGNee6e261ad0d1418832cc48a696e4895e sio:SIO_000628 miriam-gene:9447, lld:C0024141; a sio:SIO_001121 . } dgn-np:NP1000978.RAp9oRsFfPz2HZ-kGxFj2S5QFPd0mFlV98IHvKj00SCyk130_provenance { dgn-np:NP1000978.RAp9oRsFfPz2HZ-kGxFj2S5QFPd0mFlV98IHvKj00SCyk130_assertion dcterms:description "[Interestingly, recent studies involving the generation of Nba2 subcongenic mouse lines and generation of mice deficient for the Fcgr2b or Aim2 gene within the interval have provided evidence that epistatic interactions among the Nba2 genes contribute to increased lupus susceptibility.]. 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:22841963; 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:NP1000978.RAp9oRsFfPz2HZ-kGxFj2S5QFPd0mFlV98IHvKj00SCyk130_publicationInfo { this: dcterms:created "2016-05-13T12:49:19+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" . }