@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP220433.RArOGmAZ_xEPeehEqpILpXFdifwhYoB_q3u_eEC0HBvuI
> .
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http://www.w3.org/2000/01/rdf-schema#
> .
@prefix xsd: <
http://www.w3.org/2001/XMLSchema#
> .
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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#
> .
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{
this:
np:hasAssertion
dgn-np:NP220433.RArOGmAZ_xEPeehEqpILpXFdifwhYoB_q3u_eEC0HBvuI130_assertion
;
np:hasProvenance
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np:hasPublicationInfo
dgn-np:NP220433.RArOGmAZ_xEPeehEqpILpXFdifwhYoB_q3u_eEC0HBvuI130_publicationInfo
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a
np:Nanopublication
.
dgn-np:NP220433.RArOGmAZ_xEPeehEqpILpXFdifwhYoB_q3u_eEC0HBvuI130_assertion
a
np:Assertion
.
dgn-np:NP220433.RArOGmAZ_xEPeehEqpILpXFdifwhYoB_q3u_eEC0HBvuI130_provenance
a
np:Provenance
.
dgn-np:NP220433.RArOGmAZ_xEPeehEqpILpXFdifwhYoB_q3u_eEC0HBvuI130_publicationInfo
a
np:PublicationInfo
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dgn-np:NP220433.RArOGmAZ_xEPeehEqpILpXFdifwhYoB_q3u_eEC0HBvuI130_assertion
{
miriam-gene:1136
a
ncit:C16612
.
lld:C0028043
a
ncit:C7057
.
dgn-gda:DGNe577b40f858d90f162b37452b144589e
sio:SIO_000628
miriam-gene:1136
,
lld:C0028043
;
a
sio:SIO_001121
.
}
dgn-np:NP220433.RArOGmAZ_xEPeehEqpILpXFdifwhYoB_q3u_eEC0HBvuI130_provenance
{
dgn-np:NP220433.RArOGmAZ_xEPeehEqpILpXFdifwhYoB_q3u_eEC0HBvuI130_assertion
dcterms:description
"[These findings suggest that SNPs in the CHRNA3 and CHRNA5 region contribute to lung cancer risk, and while variant alleles are less frequent in African Americans, risk in this group may be greater than in whites and less likely to reflect an indirect effect on lung cancer risk through nicotine dependence.]. 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:19641473
;
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:NP220433.RArOGmAZ_xEPeehEqpILpXFdifwhYoB_q3u_eEC0HBvuI130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:02+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
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pav:authoredBy
<
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> , <
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http://orcid.org/0000-0002-9383-528X
> , <
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http://orcid.org/0000-0003-1244-7654
> ;
pav:createdBy
<
http://orcid.org/0000-0003-0169-8159
> ;
pav:version
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"v2.1.0" .
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