@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:NP850249.RA4RxehoOuPHKbXcl2sYx9_bN2aH6FkJToB8hW_MHy0zY130_head { this: np:hasAssertion dgn-np:NP850249.RA4RxehoOuPHKbXcl2sYx9_bN2aH6FkJToB8hW_MHy0zY130_assertion; np:hasProvenance dgn-np:NP850249.RA4RxehoOuPHKbXcl2sYx9_bN2aH6FkJToB8hW_MHy0zY130_provenance; np:hasPublicationInfo dgn-np:NP850249.RA4RxehoOuPHKbXcl2sYx9_bN2aH6FkJToB8hW_MHy0zY130_publicationInfo; a np:Nanopublication . dgn-np:NP850249.RA4RxehoOuPHKbXcl2sYx9_bN2aH6FkJToB8hW_MHy0zY130_assertion a np:Assertion . dgn-np:NP850249.RA4RxehoOuPHKbXcl2sYx9_bN2aH6FkJToB8hW_MHy0zY130_provenance a np:Provenance . dgn-np:NP850249.RA4RxehoOuPHKbXcl2sYx9_bN2aH6FkJToB8hW_MHy0zY130_publicationInfo a np:PublicationInfo . } dgn-np:NP850249.RA4RxehoOuPHKbXcl2sYx9_bN2aH6FkJToB8hW_MHy0zY130_assertion { miriam-gene:8266 a ncit:C16612 . lld:C0149676 a ncit:C7057 . dgn-gda:DGNf278fb74f17ace72e998722f68e30b4c sio:SIO_000628 miriam-gene:8266, lld:C0149676; a sio:SIO_001121 . } dgn-np:NP850249.RA4RxehoOuPHKbXcl2sYx9_bN2aH6FkJToB8hW_MHy0zY130_provenance { dgn-np:NP850249.RA4RxehoOuPHKbXcl2sYx9_bN2aH6FkJToB8hW_MHy0zY130_assertion dcterms:description "[Screening for both mutations associated with enzyme deficiency and silent polymorphisms at the G-6-PD gene was performed in the enzyme-deficient individuals by PCR-SSCP combined with restriction enzyme analysis; the silent polymorphisms as well as the nondeficient variant G-6-PD A(376G) were also investigated in 366 G-6-PD normal individuals from the general population.]. 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:12367588; prov:wasDerivedFrom dgn-void:befree-20140225; prov:wasGeneratedBy eco:ECO_0000203 . dgn-void:befree-20140225 pav:importedOn "2014-02-25"^^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:NP850249.RA4RxehoOuPHKbXcl2sYx9_bN2aH6FkJToB8hW_MHy0zY130_publicationInfo { this: dcterms:created "2014-10-02T12:40:39+02:00"^^xsd:dateTime; dcterms:rights ; dcterms:rightsHolder dgn-void:IBIGroup; dcterms:subject sio:SIO_000983; prv:usedData dgn-void:disgenetrdf; pav:authoredBy , , , , ; pav:createdBy ; pav:version "v2.1.0.0" . dgn-void:disgenetrdf pav:version "v2.1.0" . }