@prefix dc: <
http://purl.org/dc/terms/
> .
@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP126152.RAlaJpaaOkP2cBRUypu1cmHXE4pnzU_938dsvrMo4mH7k
> .
@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 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:NP126152.RAlaJpaaOkP2cBRUypu1cmHXE4pnzU_938dsvrMo4mH7k130_head
{
this:
np:hasAssertion
dgn-np:NP126152.RAlaJpaaOkP2cBRUypu1cmHXE4pnzU_938dsvrMo4mH7k130_assertion
;
np:hasProvenance
dgn-np:NP126152.RAlaJpaaOkP2cBRUypu1cmHXE4pnzU_938dsvrMo4mH7k130_provenance
;
np:hasPublicationInfo
dgn-np:NP126152.RAlaJpaaOkP2cBRUypu1cmHXE4pnzU_938dsvrMo4mH7k130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP126152.RAlaJpaaOkP2cBRUypu1cmHXE4pnzU_938dsvrMo4mH7k130_assertion
a
np:Assertion
.
dgn-np:NP126152.RAlaJpaaOkP2cBRUypu1cmHXE4pnzU_938dsvrMo4mH7k130_provenance
a
np:Provenance
.
dgn-np:NP126152.RAlaJpaaOkP2cBRUypu1cmHXE4pnzU_938dsvrMo4mH7k130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP126152.RAlaJpaaOkP2cBRUypu1cmHXE4pnzU_938dsvrMo4mH7k130_assertion
{
miriam-gene:2067
a
ncit:C16612
.
lld:C0919267
a
ncit:C7057
.
dgn-gda:DGN9e59980703953c08ece343f6c9686aac
sio:SIO_000628
miriam-gene:2067
,
lld:C0919267
;
a
sio:SIO_001122
.
}
dgn-np:NP126152.RAlaJpaaOkP2cBRUypu1cmHXE4pnzU_938dsvrMo4mH7k130_provenance
{
dgn-np:NP126152.RAlaJpaaOkP2cBRUypu1cmHXE4pnzU_938dsvrMo4mH7k130_assertion
dc:description
"[Although the ERCC1 codon 118 polymorphism does not seem to be associated with clinical outcome, the C8092A polymorphism was an independent predictor of survivalin women with optimally resected stage III epithelial ovarian cancer ]. 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:18640939
;
prov:wasDerivedFrom
dgn-void:lhgdn-20090331
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:lhgdn-20090331
pav:importedOn
"2009-03-31"^^
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:NP126152.RAlaJpaaOkP2cBRUypu1cmHXE4pnzU_938dsvrMo4mH7k130_publicationInfo
{
this:
dc:created
"2014-10-02T12:33:05+02:00"^^
xsd:dateTime
;
dc:rights
<
http://opendatacommons.org/licenses/odbl/1.0/
> ;
dc:rightsHolder
dgn-void:IBIGroup
;
dc: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" .
}