@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:NP408722.RAkKwAVx5J7jprfdaTLo5XCqLGUuZcLWKQcXsbizJWX30130_head { this: np:hasAssertion dgn-np:NP408722.RAkKwAVx5J7jprfdaTLo5XCqLGUuZcLWKQcXsbizJWX30130_assertion; np:hasProvenance dgn-np:NP408722.RAkKwAVx5J7jprfdaTLo5XCqLGUuZcLWKQcXsbizJWX30130_provenance; np:hasPublicationInfo dgn-np:NP408722.RAkKwAVx5J7jprfdaTLo5XCqLGUuZcLWKQcXsbizJWX30130_publicationInfo; a np:Nanopublication . dgn-np:NP408722.RAkKwAVx5J7jprfdaTLo5XCqLGUuZcLWKQcXsbizJWX30130_assertion a np:Assertion . dgn-np:NP408722.RAkKwAVx5J7jprfdaTLo5XCqLGUuZcLWKQcXsbizJWX30130_provenance a np:Provenance . dgn-np:NP408722.RAkKwAVx5J7jprfdaTLo5XCqLGUuZcLWKQcXsbizJWX30130_publicationInfo a np:PublicationInfo . } dgn-np:NP408722.RAkKwAVx5J7jprfdaTLo5XCqLGUuZcLWKQcXsbizJWX30130_assertion { miriam-gene:2539 a ncit:C16612 . lld:C2939465 a ncit:C7057 . dgn-gda:DGN40b5ee68982c14b0a1d0fab98a9cbf2f sio:SIO_000628 miriam-gene:2539, lld:C2939465; a sio:SIO_001121 . } dgn-np:NP408722.RAkKwAVx5J7jprfdaTLo5XCqLGUuZcLWKQcXsbizJWX30130_provenance { dgn-np:NP408722.RAkKwAVx5J7jprfdaTLo5XCqLGUuZcLWKQcXsbizJWX30130_assertion dcterms:description "[The aim of the study was to determine whether the routine semiquantitative fluorescent spot test could detect all cases of G6PD deficiency, including those cases with partial deficiency (residual red cell G6PD activity between 20-60% of normal).]. 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:12971572; 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:NP408722.RAkKwAVx5J7jprfdaTLo5XCqLGUuZcLWKQcXsbizJWX30130_publicationInfo { this: dcterms:created "2016-05-13T12:44:50+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" . }