@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP59333.RARNlEq3U3NBCdBIE7kJTotxZnaln3BnbLR0xkaAo5ew0
> .
@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:NP59333.RARNlEq3U3NBCdBIE7kJTotxZnaln3BnbLR0xkaAo5ew0130_head
{
this:
np:hasAssertion
dgn-np:NP59333.RARNlEq3U3NBCdBIE7kJTotxZnaln3BnbLR0xkaAo5ew0130_assertion
;
np:hasProvenance
dgn-np:NP59333.RARNlEq3U3NBCdBIE7kJTotxZnaln3BnbLR0xkaAo5ew0130_provenance
;
np:hasPublicationInfo
dgn-np:NP59333.RARNlEq3U3NBCdBIE7kJTotxZnaln3BnbLR0xkaAo5ew0130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP59333.RARNlEq3U3NBCdBIE7kJTotxZnaln3BnbLR0xkaAo5ew0130_assertion
a
np:Assertion
.
dgn-np:NP59333.RARNlEq3U3NBCdBIE7kJTotxZnaln3BnbLR0xkaAo5ew0130_provenance
a
np:Provenance
.
dgn-np:NP59333.RARNlEq3U3NBCdBIE7kJTotxZnaln3BnbLR0xkaAo5ew0130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP59333.RARNlEq3U3NBCdBIE7kJTotxZnaln3BnbLR0xkaAo5ew0130_assertion
{
miriam-gene:7508
a
ncit:C16612
.
lld:C0242379
a
ncit:C7057
.
dgn-gda:DGNbfcfa2865f53a2d54fc882156404005a
sio:SIO_000628
miriam-gene:7508
,
lld:C0242379
;
a
sio:SIO_001122
.
}
dgn-np:NP59333.RARNlEq3U3NBCdBIE7kJTotxZnaln3BnbLR0xkaAo5ew0130_provenance
{
dgn-np:NP59333.RARNlEq3U3NBCdBIE7kJTotxZnaln3BnbLR0xkaAo5ew0130_assertion
dcterms:description
"[These findings indicate that XPC exonic variants may contribute to the risk of lung cancer in the Chinese population, and these variant genotypes may modulate the risk of lung cancer associated with 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:15700316
;
prov:wasDerivedFrom
dgn-void:gad-20130706
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:gad-20130706
pav:importedOn
"2013-07-06"^^
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:NP59333.RARNlEq3U3NBCdBIE7kJTotxZnaln3BnbLR0xkaAo5ew0130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:28+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" .
}