@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP582251.RAmbWJa-qHj1dWjCI-qPKaV2Iw0SArn40qDsWTqrt0KnE
> .
@prefix rdfs: <
http://www.w3.org/2000/01/rdf-schema#
> .
@prefix xsd: <
http://www.w3.org/2001/XMLSchema#
> .
@prefix sio: <
http://semanticscience.org/resource/
> .
@prefix ncit: <
http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#
> .
@prefix lld: <
http://linkedlifedata.com/resource/umls/id/
> .
@prefix miriam-gene: <
http://identifiers.org/ncbigene/
> .
@prefix miriam-pubmed: <
http://identifiers.org/pubmed/
> .
@prefix eco: <
http://purl.obolibrary.org/obo/eco.owl#
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/2.0/
> .
@prefix prv: <
http://purl.org/net/provenance/ns#
> .
@prefix dcterms: <
http://purl.org/dc/terms/
> .
@prefix np: <
http://www.nanopub.org/nschema#
> .
@prefix dgn-np: <
http://rdf.disgenet.org/nanopublications.trig#
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/gene-disease-association.ttl#
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v2.1.0/void.ttl#
> .
dgn-np:NP582251.RAmbWJa-qHj1dWjCI-qPKaV2Iw0SArn40qDsWTqrt0KnE130_head
{
this:
np:hasAssertion
dgn-np:NP582251.RAmbWJa-qHj1dWjCI-qPKaV2Iw0SArn40qDsWTqrt0KnE130_assertion
;
np:hasProvenance
dgn-np:NP582251.RAmbWJa-qHj1dWjCI-qPKaV2Iw0SArn40qDsWTqrt0KnE130_provenance
;
np:hasPublicationInfo
dgn-np:NP582251.RAmbWJa-qHj1dWjCI-qPKaV2Iw0SArn40qDsWTqrt0KnE130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP582251.RAmbWJa-qHj1dWjCI-qPKaV2Iw0SArn40qDsWTqrt0KnE130_assertion
a
np:Assertion
.
dgn-np:NP582251.RAmbWJa-qHj1dWjCI-qPKaV2Iw0SArn40qDsWTqrt0KnE130_provenance
a
np:Provenance
.
dgn-np:NP582251.RAmbWJa-qHj1dWjCI-qPKaV2Iw0SArn40qDsWTqrt0KnE130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP582251.RAmbWJa-qHj1dWjCI-qPKaV2Iw0SArn40qDsWTqrt0KnE130_assertion
{
miriam-gene:1728
a
ncit:C16612
.
lld:C0023467
a
ncit:C7057
.
dgn-gda:DGN3ff1a36be26a95aad8c869a9eaffe9a9
sio:SIO_000628
miriam-gene:1728
,
lld:C0023467
;
a
sio:SIO_001121
.
}
dgn-np:NP582251.RAmbWJa-qHj1dWjCI-qPKaV2Iw0SArn40qDsWTqrt0KnE130_provenance
{
dgn-np:NP582251.RAmbWJa-qHj1dWjCI-qPKaV2Iw0SArn40qDsWTqrt0KnE130_assertion
dcterms:description
"[We analyzed NQO1 C609T gene polymorphism using the PCR-RFLP method in 273 patients with de novo acute leukemia (189 acute lymphoblastic leukemia (ALL), and 84 acute myeloid leukemia (AML) and 286 healthy volunteers to investigate the role of NQO1 polymorphism in the etiology of acute leukemia.]. 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:15382274
;
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:NP582251.RAmbWJa-qHj1dWjCI-qPKaV2Iw0SArn40qDsWTqrt0KnE130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:50+02:00"^^
xsd:dateTime
;
dcterms:rights
<
http://opendatacommons.org/licenses/odbl/1.0/
> ;
dcterms:rightsHolder
dgn-void:IBIGroup
;
dcterms:subject
sio:SIO_000983
;
prv:usedData
dgn-void:disgenetrdf
;
pav:authoredBy
<
http://orcid.org/0000-0001-5999-6269
> , <
http://orcid.org/0000-0002-7534-7661
> , <
http://orcid.org/0000-0002-9383-528X
> , <
http://orcid.org/0000-0003-0169-8159
> , <
http://orcid.org/0000-0003-1244-7654
> ;
pav:createdBy
<
http://orcid.org/0000-0003-0169-8159
> ;
pav:version
"v2.1.0.0" .
dgn-void:disgenetrdf
pav:version
"v2.1.0" .
}