@prefix dct: .
@prefix ns1: .
@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 np: .
@prefix dgn-gda: .
@prefix dgn-void: .
ns1:NP1412915.RA7cFiuUJZjqtIktH3y_8EgwbnQLyMT5QXi28zu9bJuc8130_head {
this: np:hasAssertion ns1:NP1412915.RA7cFiuUJZjqtIktH3y_8EgwbnQLyMT5QXi28zu9bJuc8130_assertion;
np:hasProvenance ns1:NP1412915.RA7cFiuUJZjqtIktH3y_8EgwbnQLyMT5QXi28zu9bJuc8130_provenance;
np:hasPublicationInfo ns1:NP1412915.RA7cFiuUJZjqtIktH3y_8EgwbnQLyMT5QXi28zu9bJuc8130_publicationInfo;
a np:Nanopublication .
ns1:NP1412915.RA7cFiuUJZjqtIktH3y_8EgwbnQLyMT5QXi28zu9bJuc8130_assertion a np:Assertion .
ns1:NP1412915.RA7cFiuUJZjqtIktH3y_8EgwbnQLyMT5QXi28zu9bJuc8130_provenance a np:Provenance .
ns1:NP1412915.RA7cFiuUJZjqtIktH3y_8EgwbnQLyMT5QXi28zu9bJuc8130_publicationInfo a np:PublicationInfo .
}
ns1:NP1412915.RA7cFiuUJZjqtIktH3y_8EgwbnQLyMT5QXi28zu9bJuc8130_assertion {
miriam-gene:2539 a ncit:C16612 .
lld:C2939465 a ncit:C7057 .
dgn-gda:DGNe83fc3e3015a8970b81db6017f6f2969 sio:SIO_000628 miriam-gene:2539, lld:C2939465;
a sio:SIO_001122 .
}
ns1:NP1412915.RA7cFiuUJZjqtIktH3y_8EgwbnQLyMT5QXi28zu9bJuc8130_provenance {
ns1:NP1412915.RA7cFiuUJZjqtIktH3y_8EgwbnQLyMT5QXi28zu9bJuc8130_assertion dct:description
"[In the present investigation, DNA samples from 17 patients with G6PD deficiency from Tianjin area in North China were studied for the two G6PD common mutations (R459L and R463H) and two single nucleotide polymorphisms (1311C/T and 1365-13T/C) using a dideoxy fingerprinting method.]. 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:9891846;
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 .
}
ns1:NP1412915.RA7cFiuUJZjqtIktH3y_8EgwbnQLyMT5QXi28zu9bJuc8130_publicationInfo {
this: dct:created "2016-05-13T12:52:27+02:00"^^xsd:dateTime;
dct:rights ;
dct:rightsHolder dgn-void:IBIGroup;
dct: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" .
}