@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP432076.RALPXFvolCFgKsWnb9KaKCe8G31oLcvMt8UiM1RMfHF0I
> .
@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:NP432076.RALPXFvolCFgKsWnb9KaKCe8G31oLcvMt8UiM1RMfHF0I130_head
{
this:
np:hasAssertion
dgn-np:NP432076.RALPXFvolCFgKsWnb9KaKCe8G31oLcvMt8UiM1RMfHF0I130_assertion
;
np:hasProvenance
dgn-np:NP432076.RALPXFvolCFgKsWnb9KaKCe8G31oLcvMt8UiM1RMfHF0I130_provenance
;
np:hasPublicationInfo
dgn-np:NP432076.RALPXFvolCFgKsWnb9KaKCe8G31oLcvMt8UiM1RMfHF0I130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP432076.RALPXFvolCFgKsWnb9KaKCe8G31oLcvMt8UiM1RMfHF0I130_assertion
a
np:Assertion
.
dgn-np:NP432076.RALPXFvolCFgKsWnb9KaKCe8G31oLcvMt8UiM1RMfHF0I130_provenance
a
np:Provenance
.
dgn-np:NP432076.RALPXFvolCFgKsWnb9KaKCe8G31oLcvMt8UiM1RMfHF0I130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP432076.RALPXFvolCFgKsWnb9KaKCe8G31oLcvMt8UiM1RMfHF0I130_assertion
{
miriam-gene:2952
a
ncit:C16612
.
lld:C1512433
a
ncit:C7057
.
dgn-gda:DGN936627508369174bf715da619909a91b
sio:SIO_000628
miriam-gene:2952
,
lld:C1512433
;
a
sio:SIO_001121
.
}
dgn-np:NP432076.RALPXFvolCFgKsWnb9KaKCe8G31oLcvMt8UiM1RMfHF0I130_provenance
{
dgn-np:NP432076.RALPXFvolCFgKsWnb9KaKCe8G31oLcvMt8UiM1RMfHF0I130_assertion
dcterms:description
"[We found the frequency of GSTT1 null in the control and case groups was not significantly different, though frequency distributions of combinations of the genotype with smoking in mutually exclusive groups in the high-grade CIN group and the other case groups were significantly different.]. 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:8001244
;
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:NP432076.RALPXFvolCFgKsWnb9KaKCe8G31oLcvMt8UiM1RMfHF0I130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:16+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" .
}