@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP673265.RAqLMMtamvcBr3w57JhhbYPTRLRK-txFwgxtJz6w1jDag
> .
@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:NP673265.RAqLMMtamvcBr3w57JhhbYPTRLRK-txFwgxtJz6w1jDag130_head
{
this:
np:hasAssertion
dgn-np:NP673265.RAqLMMtamvcBr3w57JhhbYPTRLRK-txFwgxtJz6w1jDag130_assertion
;
np:hasProvenance
dgn-np:NP673265.RAqLMMtamvcBr3w57JhhbYPTRLRK-txFwgxtJz6w1jDag130_provenance
;
np:hasPublicationInfo
dgn-np:NP673265.RAqLMMtamvcBr3w57JhhbYPTRLRK-txFwgxtJz6w1jDag130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP673265.RAqLMMtamvcBr3w57JhhbYPTRLRK-txFwgxtJz6w1jDag130_assertion
a
np:Assertion
.
dgn-np:NP673265.RAqLMMtamvcBr3w57JhhbYPTRLRK-txFwgxtJz6w1jDag130_provenance
a
np:Provenance
.
dgn-np:NP673265.RAqLMMtamvcBr3w57JhhbYPTRLRK-txFwgxtJz6w1jDag130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP673265.RAqLMMtamvcBr3w57JhhbYPTRLRK-txFwgxtJz6w1jDag130_assertion
{
miriam-gene:196
a
ncit:C16612
.
lld:C0017638
a
ncit:C7057
.
dgn-gda:DGN7c726cced78234b40d1074ad616eddb4
sio:SIO_000628
miriam-gene:196
,
lld:C0017638
;
a
sio:SIO_001121
.
}
dgn-np:NP673265.RAqLMMtamvcBr3w57JhhbYPTRLRK-txFwgxtJz6w1jDag130_provenance
{
dgn-np:NP673265.RAqLMMtamvcBr3w57JhhbYPTRLRK-txFwgxtJz6w1jDag130_assertion
dcterms:description
"[Further studies with a larger sample size and ethnically diverse populations are required to elucidate the potential biological mechanism for, as well as the impact of, the susceptibility to glioma due to genetic variants of AHR.]. 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:22539616
;
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:NP673265.RAqLMMtamvcBr3w57JhhbYPTRLRK-txFwgxtJz6w1jDag130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:46+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" .
}