@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP340580.RADzuaX7HiDfGZzi7-4uChWLBACuzquSn54gAa6J3vnWY
> .
@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:NP340580.RADzuaX7HiDfGZzi7-4uChWLBACuzquSn54gAa6J3vnWY130_head
{
this:
np:hasAssertion
dgn-np:NP340580.RADzuaX7HiDfGZzi7-4uChWLBACuzquSn54gAa6J3vnWY130_assertion
;
np:hasProvenance
dgn-np:NP340580.RADzuaX7HiDfGZzi7-4uChWLBACuzquSn54gAa6J3vnWY130_provenance
;
np:hasPublicationInfo
dgn-np:NP340580.RADzuaX7HiDfGZzi7-4uChWLBACuzquSn54gAa6J3vnWY130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP340580.RADzuaX7HiDfGZzi7-4uChWLBACuzquSn54gAa6J3vnWY130_assertion
a
np:Assertion
.
dgn-np:NP340580.RADzuaX7HiDfGZzi7-4uChWLBACuzquSn54gAa6J3vnWY130_provenance
a
np:Provenance
.
dgn-np:NP340580.RADzuaX7HiDfGZzi7-4uChWLBACuzquSn54gAa6J3vnWY130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP340580.RADzuaX7HiDfGZzi7-4uChWLBACuzquSn54gAa6J3vnWY130_assertion
{
miriam-gene:5241
a
ncit:C16612
.
lld:C0677886
a
ncit:C7057
.
dgn-gda:DGN03e1962dd97ae6627925ee73fda6fed8
sio:SIO_000628
miriam-gene:5241
,
lld:C0677886
;
a
sio:SIO_001121
.
}
dgn-np:NP340580.RADzuaX7HiDfGZzi7-4uChWLBACuzquSn54gAa6J3vnWY130_provenance
{
dgn-np:NP340580.RADzuaX7HiDfGZzi7-4uChWLBACuzquSn54gAa6J3vnWY130_assertion
dcterms:description
"[To assess whether the progesterone receptor (PR) exon 4 valine to leucine amino acid variant is associated with specific tumour characteristics or with overall risk of ovarian cancer, we examined 551 cases of epithelial ovarian cancer and 298 unaffected controls for the underlying G-->T nucleotide substitution polymorphism.]. 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:11323389
;
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:NP340580.RADzuaX7HiDfGZzi7-4uChWLBACuzquSn54gAa6J3vnWY130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:20+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" .
}