@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:NP440020.RAI0RBiOwxKFE44DZEQUkJc4VHitlX_kt3UCe4DtfxsNo130_head { this: np:hasAssertion dgn-np:NP440020.RAI0RBiOwxKFE44DZEQUkJc4VHitlX_kt3UCe4DtfxsNo130_assertion; np:hasProvenance dgn-np:NP440020.RAI0RBiOwxKFE44DZEQUkJc4VHitlX_kt3UCe4DtfxsNo130_provenance; np:hasPublicationInfo dgn-np:NP440020.RAI0RBiOwxKFE44DZEQUkJc4VHitlX_kt3UCe4DtfxsNo130_publicationInfo; a np:Nanopublication . dgn-np:NP440020.RAI0RBiOwxKFE44DZEQUkJc4VHitlX_kt3UCe4DtfxsNo130_assertion a np:Assertion . dgn-np:NP440020.RAI0RBiOwxKFE44DZEQUkJc4VHitlX_kt3UCe4DtfxsNo130_provenance a np:Provenance . dgn-np:NP440020.RAI0RBiOwxKFE44DZEQUkJc4VHitlX_kt3UCe4DtfxsNo130_publicationInfo a np:PublicationInfo . } dgn-np:NP440020.RAI0RBiOwxKFE44DZEQUkJc4VHitlX_kt3UCe4DtfxsNo130_assertion { miriam-gene:2952 a ncit:C16612 . lld:C0004096 a ncit:C7057 . dgn-gda:DGN8ca8917c80d8236181274c80a8a98825 sio:SIO_000628 miriam-gene:2952, lld:C0004096; a sio:SIO_001121 . } dgn-np:NP440020.RAI0RBiOwxKFE44DZEQUkJc4VHitlX_kt3UCe4DtfxsNo130_provenance { dgn-np:NP440020.RAI0RBiOwxKFE44DZEQUkJc4VHitlX_kt3UCe4DtfxsNo130_assertion dcterms:description "[The significant detection of GSTT1 null genotype more in controls than in asthmatics with no association with other atopic manifestations or asthma severity and the lack of association detected between GSTM1 polymorphism in relation to asthma, atopy or asthma severity confirm the uncertain role of those genes in the development of asthma.]. 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:24559168; 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:NP440020.RAI0RBiOwxKFE44DZEQUkJc4VHitlX_kt3UCe4DtfxsNo130_publicationInfo { this: dcterms:created "2015-08-25T14:41:57+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" . }