@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP822574.RAvZocNUHNt52zda14VMY_6392_MBD1Dk-zlpDgXUHPQE
> .
@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:NP822574.RAvZocNUHNt52zda14VMY_6392_MBD1Dk-zlpDgXUHPQE130_head
{
this:
np:hasAssertion
dgn-np:NP822574.RAvZocNUHNt52zda14VMY_6392_MBD1Dk-zlpDgXUHPQE130_assertion
;
np:hasProvenance
dgn-np:NP822574.RAvZocNUHNt52zda14VMY_6392_MBD1Dk-zlpDgXUHPQE130_provenance
;
np:hasPublicationInfo
dgn-np:NP822574.RAvZocNUHNt52zda14VMY_6392_MBD1Dk-zlpDgXUHPQE130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP822574.RAvZocNUHNt52zda14VMY_6392_MBD1Dk-zlpDgXUHPQE130_assertion
a
np:Assertion
.
dgn-np:NP822574.RAvZocNUHNt52zda14VMY_6392_MBD1Dk-zlpDgXUHPQE130_provenance
a
np:Provenance
.
dgn-np:NP822574.RAvZocNUHNt52zda14VMY_6392_MBD1Dk-zlpDgXUHPQE130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP822574.RAvZocNUHNt52zda14VMY_6392_MBD1Dk-zlpDgXUHPQE130_assertion
{
miriam-gene:3294
a
ncit:C16612
.
lld:C0009402
a
ncit:C7057
.
dgn-gda:DGNf997d1cee117d472ccd928f95c0e2d67
sio:SIO_000628
miriam-gene:3294
,
lld:C0009402
;
a
sio:SIO_001121
.
}
dgn-np:NP822574.RAvZocNUHNt52zda14VMY_6392_MBD1Dk-zlpDgXUHPQE130_provenance
{
dgn-np:NP822574.RAvZocNUHNt52zda14VMY_6392_MBD1Dk-zlpDgXUHPQE130_assertion
dcterms:description
"[We conducted a comprehensive evaluation of single nucleotide polymorphisms (SNPs) in genes encoding 3 hormone receptors (ESR1, ESR2, PGR) and 5 hormone synthesizers (CYP19A1 and CYP17A1, HSD17B1, HSD17B2, HSD17B4) among 427 women with incident colorectal cancer and 871 matched controls who were Caucasians of European ancestry from 93676 postmenopausal women enrolled in the Women's Health Initiative Observational cohort.]. 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:21627810
;
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:NP822574.RAvZocNUHNt52zda14VMY_6392_MBD1Dk-zlpDgXUHPQE130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:24+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" .
}