@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP225177.RA8NLy5K7kJYzkQ0Q9VxpsMW-MpIn55UzcAXMAyoCLpig
> .
@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:NP225177.RA8NLy5K7kJYzkQ0Q9VxpsMW-MpIn55UzcAXMAyoCLpig130_head
{
this:
np:hasAssertion
dgn-np:NP225177.RA8NLy5K7kJYzkQ0Q9VxpsMW-MpIn55UzcAXMAyoCLpig130_assertion
;
np:hasProvenance
dgn-np:NP225177.RA8NLy5K7kJYzkQ0Q9VxpsMW-MpIn55UzcAXMAyoCLpig130_provenance
;
np:hasPublicationInfo
dgn-np:NP225177.RA8NLy5K7kJYzkQ0Q9VxpsMW-MpIn55UzcAXMAyoCLpig130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP225177.RA8NLy5K7kJYzkQ0Q9VxpsMW-MpIn55UzcAXMAyoCLpig130_assertion
a
np:Assertion
.
dgn-np:NP225177.RA8NLy5K7kJYzkQ0Q9VxpsMW-MpIn55UzcAXMAyoCLpig130_provenance
a
np:Provenance
.
dgn-np:NP225177.RA8NLy5K7kJYzkQ0Q9VxpsMW-MpIn55UzcAXMAyoCLpig130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP225177.RA8NLy5K7kJYzkQ0Q9VxpsMW-MpIn55UzcAXMAyoCLpig130_assertion
{
miriam-gene:1553
a
ncit:C16612
.
lld:C0684249
a
ncit:C7057
.
dgn-gda:DGNbd126769b66a4c04c12a48d8ca908d26
sio:SIO_000628
miriam-gene:1553
,
lld:C0684249
;
a
sio:SIO_001121
.
}
dgn-np:NP225177.RA8NLy5K7kJYzkQ0Q9VxpsMW-MpIn55UzcAXMAyoCLpig130_provenance
{
dgn-np:NP225177.RA8NLy5K7kJYzkQ0Q9VxpsMW-MpIn55UzcAXMAyoCLpig130_assertion
dcterms:description
"[In this case-control study, we genotyped 724 patients with lung cancer and 791 controls for this polymorphism to examine the hypothesis that the variant CYP2A13 may have impact on risk of lung cancer in relation to tobacco smoking.]. 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:14633739
;
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:NP225177.RA8NLy5K7kJYzkQ0Q9VxpsMW-MpIn55UzcAXMAyoCLpig130_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" .
}