@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP224946.RAm3cVZgWUV4rUbupe37HrgiIfdeZlujcYjmEj3nV1IgE
> .
@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:NP224946.RAm3cVZgWUV4rUbupe37HrgiIfdeZlujcYjmEj3nV1IgE130_head
{
this:
np:hasAssertion
dgn-np:NP224946.RAm3cVZgWUV4rUbupe37HrgiIfdeZlujcYjmEj3nV1IgE130_assertion
;
np:hasProvenance
dgn-np:NP224946.RAm3cVZgWUV4rUbupe37HrgiIfdeZlujcYjmEj3nV1IgE130_provenance
;
np:hasPublicationInfo
dgn-np:NP224946.RAm3cVZgWUV4rUbupe37HrgiIfdeZlujcYjmEj3nV1IgE130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP224946.RAm3cVZgWUV4rUbupe37HrgiIfdeZlujcYjmEj3nV1IgE130_assertion
a
np:Assertion
.
dgn-np:NP224946.RAm3cVZgWUV4rUbupe37HrgiIfdeZlujcYjmEj3nV1IgE130_provenance
a
np:Provenance
.
dgn-np:NP224946.RAm3cVZgWUV4rUbupe37HrgiIfdeZlujcYjmEj3nV1IgE130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP224946.RAm3cVZgWUV4rUbupe37HrgiIfdeZlujcYjmEj3nV1IgE130_assertion
{
miriam-gene:2952
a
ncit:C16612
.
lld:C0684249
a
ncit:C7057
.
dgn-gda:DGN1a6bf56a70afcb2203afe2cad0f7bebb
sio:SIO_000628
miriam-gene:2952
,
lld:C0684249
;
a
sio:SIO_001121
.
}
dgn-np:NP224946.RAm3cVZgWUV4rUbupe37HrgiIfdeZlujcYjmEj3nV1IgE130_provenance
{
dgn-np:NP224946.RAm3cVZgWUV4rUbupe37HrgiIfdeZlujcYjmEj3nV1IgE130_assertion
dcterms:description
"[Logistic regression models showed the OR for the association of lung cancer and the presence of both null polymorphisms compared with one (either GSTT1 or GSTM1) or no null genotype to be 2.9 (P < 0.04).]. 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:9242470
;
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:NP224946.RAm3cVZgWUV4rUbupe37HrgiIfdeZlujcYjmEj3nV1IgE130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:05+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" .
}