@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:NP453814.RAnoaqfmjiz9Vg9H8HwrK9oWQQM2Uz4AEL2HU1VrxVJkU130_head { this: np:hasAssertion dgn-np:NP453814.RAnoaqfmjiz9Vg9H8HwrK9oWQQM2Uz4AEL2HU1VrxVJkU130_assertion; np:hasProvenance dgn-np:NP453814.RAnoaqfmjiz9Vg9H8HwrK9oWQQM2Uz4AEL2HU1VrxVJkU130_provenance; np:hasPublicationInfo dgn-np:NP453814.RAnoaqfmjiz9Vg9H8HwrK9oWQQM2Uz4AEL2HU1VrxVJkU130_publicationInfo; a np:Nanopublication . dgn-np:NP453814.RAnoaqfmjiz9Vg9H8HwrK9oWQQM2Uz4AEL2HU1VrxVJkU130_assertion a np:Assertion . dgn-np:NP453814.RAnoaqfmjiz9Vg9H8HwrK9oWQQM2Uz4AEL2HU1VrxVJkU130_provenance a np:Provenance . dgn-np:NP453814.RAnoaqfmjiz9Vg9H8HwrK9oWQQM2Uz4AEL2HU1VrxVJkU130_publicationInfo a np:PublicationInfo . } dgn-np:NP453814.RAnoaqfmjiz9Vg9H8HwrK9oWQQM2Uz4AEL2HU1VrxVJkU130_assertion { miriam-gene:2539 a ncit:C16612 . lld:C2939465 a ncit:C7057 . dgn-gda:DGN6230e20048e1a1ef3a08a7d1988506fe sio:SIO_000628 miriam-gene:2539, lld:C2939465; a sio:SIO_001121 . } dgn-np:NP453814.RAnoaqfmjiz9Vg9H8HwrK9oWQQM2Uz4AEL2HU1VrxVJkU130_provenance { dgn-np:NP453814.RAnoaqfmjiz9Vg9H8HwrK9oWQQM2Uz4AEL2HU1VrxVJkU130_assertion dcterms:description "[Setting up a simple and accurate method for detecting these mutations is not only useful for diagnosing G6PD deficiency under some circumstances that it is difficult to measure the activity of the enzyme, but also for studying the frequency of the G6PD genotypes.]. 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:15282679; 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:NP453814.RAnoaqfmjiz9Vg9H8HwrK9oWQQM2Uz4AEL2HU1VrxVJkU130_publicationInfo { this: dcterms:created "2016-05-13T12:45:10+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" . }