@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:NP1344539.RAfc7W9GPqUXI89GDKkP4iPHBj0jzhIuoK8SEkQFYN3B0130_head { this: np:hasAssertion dgn-np:NP1344539.RAfc7W9GPqUXI89GDKkP4iPHBj0jzhIuoK8SEkQFYN3B0130_assertion; np:hasProvenance dgn-np:NP1344539.RAfc7W9GPqUXI89GDKkP4iPHBj0jzhIuoK8SEkQFYN3B0130_provenance; np:hasPublicationInfo dgn-np:NP1344539.RAfc7W9GPqUXI89GDKkP4iPHBj0jzhIuoK8SEkQFYN3B0130_publicationInfo; a np:Nanopublication . dgn-np:NP1344539.RAfc7W9GPqUXI89GDKkP4iPHBj0jzhIuoK8SEkQFYN3B0130_assertion a np:Assertion . dgn-np:NP1344539.RAfc7W9GPqUXI89GDKkP4iPHBj0jzhIuoK8SEkQFYN3B0130_provenance a np:Provenance . dgn-np:NP1344539.RAfc7W9GPqUXI89GDKkP4iPHBj0jzhIuoK8SEkQFYN3B0130_publicationInfo a np:PublicationInfo . } dgn-np:NP1344539.RAfc7W9GPqUXI89GDKkP4iPHBj0jzhIuoK8SEkQFYN3B0130_assertion { miriam-gene:2539 a ncit:C16612 . lld:C2939465 a ncit:C7057 . dgn-gda:DGN11c1f87b66b175acbf5b364156d21a95 sio:SIO_000628 miriam-gene:2539, lld:C2939465; a sio:SIO_001122 . } dgn-np:NP1344539.RAfc7W9GPqUXI89GDKkP4iPHBj0jzhIuoK8SEkQFYN3B0130_provenance { dgn-np:NP1344539.RAfc7W9GPqUXI89GDKkP4iPHBj0jzhIuoK8SEkQFYN3B0130_assertion dcterms:description "[Remarkably, a previously unreported deficient variant, G6PD Orissa (44 Ala-->Gly), is responsible for most of the G6PD deficiency in tribal Indian populations but is not found in urban populations, where most of the G6PD deficiency is due to the G6PD Mediterranean (188 Ser-->Phe) variant.]. 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:8533762; 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:NP1344539.RAfc7W9GPqUXI89GDKkP4iPHBj0jzhIuoK8SEkQFYN3B0130_publicationInfo { this: dcterms:created "2016-05-13T12:51:55+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" . }