@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP568251.RA6duf6cjdOtGvcCyHXMqTv2A8mDOl-2m2-j5fFCTIFDY
> .
@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:NP568251.RA6duf6cjdOtGvcCyHXMqTv2A8mDOl-2m2-j5fFCTIFDY130_head
{
this:
np:hasAssertion
dgn-np:NP568251.RA6duf6cjdOtGvcCyHXMqTv2A8mDOl-2m2-j5fFCTIFDY130_assertion
;
np:hasProvenance
dgn-np:NP568251.RA6duf6cjdOtGvcCyHXMqTv2A8mDOl-2m2-j5fFCTIFDY130_provenance
;
np:hasPublicationInfo
dgn-np:NP568251.RA6duf6cjdOtGvcCyHXMqTv2A8mDOl-2m2-j5fFCTIFDY130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP568251.RA6duf6cjdOtGvcCyHXMqTv2A8mDOl-2m2-j5fFCTIFDY130_assertion
a
np:Assertion
.
dgn-np:NP568251.RA6duf6cjdOtGvcCyHXMqTv2A8mDOl-2m2-j5fFCTIFDY130_provenance
a
np:Provenance
.
dgn-np:NP568251.RA6duf6cjdOtGvcCyHXMqTv2A8mDOl-2m2-j5fFCTIFDY130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP568251.RA6duf6cjdOtGvcCyHXMqTv2A8mDOl-2m2-j5fFCTIFDY130_assertion
{
miriam-gene:2944
a
ncit:C16612
.
lld:C2931822
a
ncit:C7057
.
dgn-gda:DGNd7f00668182b139d01f267c66018ec5d
sio:SIO_000628
miriam-gene:2944
,
lld:C2931822
;
a
sio:SIO_001121
.
}
dgn-np:NP568251.RA6duf6cjdOtGvcCyHXMqTv2A8mDOl-2m2-j5fFCTIFDY130_provenance
{
dgn-np:NP568251.RA6duf6cjdOtGvcCyHXMqTv2A8mDOl-2m2-j5fFCTIFDY130_assertion
dcterms:description
"[To explore possible joint effects of the GSTM1- and GSTT1-null polymorphisms with each other and with other risk factors for nasopharyngeal carcinoma, we examined the association between each combined genotype and the risk for nasopharyngeal carcinoma stratified by gender and EBV replication status.]. 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:18628429
;
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:NP568251.RA6duf6cjdOtGvcCyHXMqTv2A8mDOl-2m2-j5fFCTIFDY130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:43+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" .
}