@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP475273.RAQvMSMFqEt_20K8f0sagHdJewk31EUnTDx_m1kkwLkD4
> .
@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:NP475273.RAQvMSMFqEt_20K8f0sagHdJewk31EUnTDx_m1kkwLkD4130_head
{
this:
np:hasAssertion
dgn-np:NP475273.RAQvMSMFqEt_20K8f0sagHdJewk31EUnTDx_m1kkwLkD4130_assertion
;
np:hasProvenance
dgn-np:NP475273.RAQvMSMFqEt_20K8f0sagHdJewk31EUnTDx_m1kkwLkD4130_provenance
;
np:hasPublicationInfo
dgn-np:NP475273.RAQvMSMFqEt_20K8f0sagHdJewk31EUnTDx_m1kkwLkD4130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP475273.RAQvMSMFqEt_20K8f0sagHdJewk31EUnTDx_m1kkwLkD4130_assertion
a
np:Assertion
.
dgn-np:NP475273.RAQvMSMFqEt_20K8f0sagHdJewk31EUnTDx_m1kkwLkD4130_provenance
a
np:Provenance
.
dgn-np:NP475273.RAQvMSMFqEt_20K8f0sagHdJewk31EUnTDx_m1kkwLkD4130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP475273.RAQvMSMFqEt_20K8f0sagHdJewk31EUnTDx_m1kkwLkD4130_assertion
{
miriam-gene:2944
a
ncit:C16612
.
lld:C0595989
a
ncit:C7057
.
dgn-gda:DGNcb2955b40f1147ff5f1cc17886302ee1
sio:SIO_000628
miriam-gene:2944
,
lld:C0595989
;
a
sio:SIO_001121
.
}
dgn-np:NP475273.RAQvMSMFqEt_20K8f0sagHdJewk31EUnTDx_m1kkwLkD4130_provenance
{
dgn-np:NP475273.RAQvMSMFqEt_20K8f0sagHdJewk31EUnTDx_m1kkwLkD4130_assertion
dcterms:description
"[The effects of the GSTM1 and GSTT1 null genotypes on laryngeal cancer risk were evaluated using peripheral blood DNA from 129 larynx cancer patients and 172 noncancer controls, all of whom were regular smokers.]. 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:9456238
;
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:NP475273.RAQvMSMFqEt_20K8f0sagHdJewk31EUnTDx_m1kkwLkD4130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:44+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" .
}