@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP208872.RA3PykE1uQv7QTeA0h5ksZSz5dKwH8oY4-qUiS5AL4b9I
> .
@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:NP208872.RA3PykE1uQv7QTeA0h5ksZSz5dKwH8oY4-qUiS5AL4b9I130_head
{
this:
np:hasAssertion
dgn-np:NP208872.RA3PykE1uQv7QTeA0h5ksZSz5dKwH8oY4-qUiS5AL4b9I130_assertion
;
np:hasProvenance
dgn-np:NP208872.RA3PykE1uQv7QTeA0h5ksZSz5dKwH8oY4-qUiS5AL4b9I130_provenance
;
np:hasPublicationInfo
dgn-np:NP208872.RA3PykE1uQv7QTeA0h5ksZSz5dKwH8oY4-qUiS5AL4b9I130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP208872.RA3PykE1uQv7QTeA0h5ksZSz5dKwH8oY4-qUiS5AL4b9I130_assertion
a
np:Assertion
.
dgn-np:NP208872.RA3PykE1uQv7QTeA0h5ksZSz5dKwH8oY4-qUiS5AL4b9I130_provenance
a
np:Provenance
.
dgn-np:NP208872.RA3PykE1uQv7QTeA0h5ksZSz5dKwH8oY4-qUiS5AL4b9I130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP208872.RA3PykE1uQv7QTeA0h5ksZSz5dKwH8oY4-qUiS5AL4b9I130_assertion
{
miriam-gene:2099
a
ncit:C16612
.
lld:C0029456
a
ncit:C7057
.
dgn-gda:DGNb8ec1ec579f04e2bd85933e68124d43e
sio:SIO_000628
miriam-gene:2099
,
lld:C0029456
;
a
sio:SIO_001121
.
}
dgn-np:NP208872.RA3PykE1uQv7QTeA0h5ksZSz5dKwH8oY4-qUiS5AL4b9I130_provenance
{
dgn-np:NP208872.RA3PykE1uQv7QTeA0h5ksZSz5dKwH8oY4-qUiS5AL4b9I130_assertion
dcterms:description
"[In view of the reported associations between osteoporosis and polymorphisms of the vitamin D receptor (VDR), collagen Ialpha1 (COLIA1) and estrogen receptor (ER) genes, an association study was performed between VDR, COLLIA1, and ER genotypes and bone mineral density, biochemical markers of bone turnover and hip fracture occurrence in Belgian older postmenopausal women.]. 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:11069192
;
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:NP208872.RA3PykE1uQv7QTeA0h5ksZSz5dKwH8oY4-qUiS5AL4b9I130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:55+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" .
}