@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP766914.RANRB7-OzzffSCT27n_1M7xNT6LUHbjGOtID2JsesdZi8
> .
@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/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@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/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v3.0.0/void/
> .
dgn-np:NP766914.RANRB7-OzzffSCT27n_1M7xNT6LUHbjGOtID2JsesdZi8130_head
{
this:
np:hasAssertion
dgn-np:NP766914.RANRB7-OzzffSCT27n_1M7xNT6LUHbjGOtID2JsesdZi8130_assertion
;
np:hasProvenance
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;
np:hasPublicationInfo
dgn-np:NP766914.RANRB7-OzzffSCT27n_1M7xNT6LUHbjGOtID2JsesdZi8130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP766914.RANRB7-OzzffSCT27n_1M7xNT6LUHbjGOtID2JsesdZi8130_assertion
a
np:Assertion
.
dgn-np:NP766914.RANRB7-OzzffSCT27n_1M7xNT6LUHbjGOtID2JsesdZi8130_provenance
a
np:Provenance
.
dgn-np:NP766914.RANRB7-OzzffSCT27n_1M7xNT6LUHbjGOtID2JsesdZi8130_publicationInfo
a
np:PublicationInfo
.
}
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{
miriam-gene:7376
a
ncit:C16612
.
lld:C0007134
a
ncit:C7057
.
dgn-gda:DGN3815ab4ed36618b2d2da3485f0ba2dbd
sio:SIO_000628
miriam-gene:7376
,
lld:C0007134
;
a
sio:SIO_001121
.
}
dgn-np:NP766914.RANRB7-OzzffSCT27n_1M7xNT6LUHbjGOtID2JsesdZi8130_provenance
{
dgn-np:NP766914.RANRB7-OzzffSCT27n_1M7xNT6LUHbjGOtID2JsesdZi8130_assertion
dcterms:description
"[In this population-based case-control study with 325 Caucasian renal cell carcinoma (RCC) patients and 335 controls matched to cases by age, gender and county of residence, we evaluated the associations between 13 potential functional polymorphisms in nine major nucleotide excision repair (NER) genes and RCC risk.]. 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:18711149
;
prov:wasDerivedFrom
dgn-void:befree-20150227
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-20150227
pav:importedOn
"2015-02-27"^^
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:NP766914.RANRB7-OzzffSCT27n_1M7xNT6LUHbjGOtID2JsesdZi8130_publicationInfo
{
this:
dcterms:created
"2015-08-25T14:45:23+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
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;
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
"v3.0.0.0" .
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pav:version
"v3.0.0" .
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