@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP495923.RAPreXTS1T8XhtnqWYR6vvPgcN7FW19JBcP-9eZ5Qmk-I
> .
@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:NP495923.RAPreXTS1T8XhtnqWYR6vvPgcN7FW19JBcP-9eZ5Qmk-I130_head
{
this:
np:hasAssertion
dgn-np:NP495923.RAPreXTS1T8XhtnqWYR6vvPgcN7FW19JBcP-9eZ5Qmk-I130_assertion
;
np:hasProvenance
dgn-np:NP495923.RAPreXTS1T8XhtnqWYR6vvPgcN7FW19JBcP-9eZ5Qmk-I130_provenance
;
np:hasPublicationInfo
dgn-np:NP495923.RAPreXTS1T8XhtnqWYR6vvPgcN7FW19JBcP-9eZ5Qmk-I130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP495923.RAPreXTS1T8XhtnqWYR6vvPgcN7FW19JBcP-9eZ5Qmk-I130_assertion
a
np:Assertion
.
dgn-np:NP495923.RAPreXTS1T8XhtnqWYR6vvPgcN7FW19JBcP-9eZ5Qmk-I130_provenance
a
np:Provenance
.
dgn-np:NP495923.RAPreXTS1T8XhtnqWYR6vvPgcN7FW19JBcP-9eZ5Qmk-I130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP495923.RAPreXTS1T8XhtnqWYR6vvPgcN7FW19JBcP-9eZ5Qmk-I130_assertion
{
miriam-gene:7421
a
ncit:C16612
.
lld:C0677886
a
ncit:C7057
.
dgn-gda:DGNc24cd8ade74e886cd0836b1b26279942
sio:SIO_000628
miriam-gene:7421
,
lld:C0677886
;
a
sio:SIO_001121
.
}
dgn-np:NP495923.RAPreXTS1T8XhtnqWYR6vvPgcN7FW19JBcP-9eZ5Qmk-I130_provenance
{
dgn-np:NP495923.RAPreXTS1T8XhtnqWYR6vvPgcN7FW19JBcP-9eZ5Qmk-I130_assertion
dcterms:description
"[Case-control data from the North Carolina Ovarian Cancer Study were analyzed using logistic regression to determine the association between seven VDR polymorphisms and EOC in both Caucasians (513 cases, 532 controls) and African Americans (74 cases, 79 controls).]. 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:23262379
;
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:NP495923.RAPreXTS1T8XhtnqWYR6vvPgcN7FW19JBcP-9eZ5Qmk-I130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:56+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" .
}