@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP779743.RAkXWfA4iw7e_uv8JFueaZdxu3l-J57wPrCEtV_xxSeOY
> .
@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:NP779743.RAkXWfA4iw7e_uv8JFueaZdxu3l-J57wPrCEtV_xxSeOY130_head
{
this:
np:hasAssertion
dgn-np:NP779743.RAkXWfA4iw7e_uv8JFueaZdxu3l-J57wPrCEtV_xxSeOY130_assertion
;
np:hasProvenance
dgn-np:NP779743.RAkXWfA4iw7e_uv8JFueaZdxu3l-J57wPrCEtV_xxSeOY130_provenance
;
np:hasPublicationInfo
dgn-np:NP779743.RAkXWfA4iw7e_uv8JFueaZdxu3l-J57wPrCEtV_xxSeOY130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP779743.RAkXWfA4iw7e_uv8JFueaZdxu3l-J57wPrCEtV_xxSeOY130_assertion
a
np:Assertion
.
dgn-np:NP779743.RAkXWfA4iw7e_uv8JFueaZdxu3l-J57wPrCEtV_xxSeOY130_provenance
a
np:Provenance
.
dgn-np:NP779743.RAkXWfA4iw7e_uv8JFueaZdxu3l-J57wPrCEtV_xxSeOY130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP779743.RAkXWfA4iw7e_uv8JFueaZdxu3l-J57wPrCEtV_xxSeOY130_assertion
{
miriam-gene:7515
a
ncit:C16612
.
lld:C0014869
a
ncit:C7057
.
dgn-gda:DGN81b53931f39dab09e32ffa654e441cfa
sio:SIO_000628
miriam-gene:7515
,
lld:C0014869
;
a
sio:SIO_001122
.
}
dgn-np:NP779743.RAkXWfA4iw7e_uv8JFueaZdxu3l-J57wPrCEtV_xxSeOY130_provenance
{
dgn-np:NP779743.RAkXWfA4iw7e_uv8JFueaZdxu3l-J57wPrCEtV_xxSeOY130_assertion
dcterms:description
"[In a population-based case-control study, we examined associations of the hOGG1 Ser 326 Cys, XRCC1 Arg 399 Gln, and XPD Lys 751 Gln polymorphisms with risk of esophageal adenocarcinoma, Barrett's esophagus, and reflux esophagitis.]. 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:18349297
;
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:NP779743.RAkXWfA4iw7e_uv8JFueaZdxu3l-J57wPrCEtV_xxSeOY130_publicationInfo
{
this:
dcterms:created
"2015-08-25T14:45:31+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:disgenetv3.0rdf
;
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" .
dgn-void:disgenetv3.0rdf
pav:version
"v3.0.0" .
}