@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP278813.RAWrYF-06EgcLO8d-sNCEz9sy3Xnl-mnyRmUz8AYP5bug
> .
@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:NP278813.RAWrYF-06EgcLO8d-sNCEz9sy3Xnl-mnyRmUz8AYP5bug130_head
{
this:
np:hasAssertion
dgn-np:NP278813.RAWrYF-06EgcLO8d-sNCEz9sy3Xnl-mnyRmUz8AYP5bug130_assertion
;
np:hasProvenance
dgn-np:NP278813.RAWrYF-06EgcLO8d-sNCEz9sy3Xnl-mnyRmUz8AYP5bug130_provenance
;
np:hasPublicationInfo
dgn-np:NP278813.RAWrYF-06EgcLO8d-sNCEz9sy3Xnl-mnyRmUz8AYP5bug130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP278813.RAWrYF-06EgcLO8d-sNCEz9sy3Xnl-mnyRmUz8AYP5bug130_assertion
a
np:Assertion
.
dgn-np:NP278813.RAWrYF-06EgcLO8d-sNCEz9sy3Xnl-mnyRmUz8AYP5bug130_provenance
a
np:Provenance
.
dgn-np:NP278813.RAWrYF-06EgcLO8d-sNCEz9sy3Xnl-mnyRmUz8AYP5bug130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP278813.RAWrYF-06EgcLO8d-sNCEz9sy3Xnl-mnyRmUz8AYP5bug130_assertion
{
miriam-gene:2068
a
ncit:C16612
.
lld:C0006826
a
ncit:C7057
.
dgn-gda:DGN60ba8a3648118ccb9fef64e07ea9705f
sio:SIO_000628
miriam-gene:2068
,
lld:C0006826
;
a
sio:SIO_001121
.
}
dgn-np:NP278813.RAWrYF-06EgcLO8d-sNCEz9sy3Xnl-mnyRmUz8AYP5bug130_provenance
{
dgn-np:NP278813.RAWrYF-06EgcLO8d-sNCEz9sy3Xnl-mnyRmUz8AYP5bug130_assertion
dcterms:description
"[The 751 Lys/Gln polymorphism of the ERCC2 gene may be linked with endometrial cancer occurrence and its effect can be potentiated by variants of the XRCC1 gene or first degree relatives positive cancer history.]. 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:22544315
;
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:NP278813.RAWrYF-06EgcLO8d-sNCEz9sy3Xnl-mnyRmUz8AYP5bug130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:37+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" .
}