@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP516494.RA1HlTc0c0EnqB0xK5nBP_5JJYKhGWxLLNx2ZfVzrqJow
> .
@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:NP516494.RA1HlTc0c0EnqB0xK5nBP_5JJYKhGWxLLNx2ZfVzrqJow130_head
{
this:
np:hasAssertion
dgn-np:NP516494.RA1HlTc0c0EnqB0xK5nBP_5JJYKhGWxLLNx2ZfVzrqJow130_assertion
;
np:hasProvenance
dgn-np:NP516494.RA1HlTc0c0EnqB0xK5nBP_5JJYKhGWxLLNx2ZfVzrqJow130_provenance
;
np:hasPublicationInfo
dgn-np:NP516494.RA1HlTc0c0EnqB0xK5nBP_5JJYKhGWxLLNx2ZfVzrqJow130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP516494.RA1HlTc0c0EnqB0xK5nBP_5JJYKhGWxLLNx2ZfVzrqJow130_assertion
a
np:Assertion
.
dgn-np:NP516494.RA1HlTc0c0EnqB0xK5nBP_5JJYKhGWxLLNx2ZfVzrqJow130_provenance
a
np:Provenance
.
dgn-np:NP516494.RA1HlTc0c0EnqB0xK5nBP_5JJYKhGWxLLNx2ZfVzrqJow130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP516494.RA1HlTc0c0EnqB0xK5nBP_5JJYKhGWxLLNx2ZfVzrqJow130_assertion
{
miriam-gene:5669
a
ncit:C16612
.
lld:C2678504
a
ncit:C7057
.
dgn-gda:DGN71146bdc15c8c056a6896cc01e7ea419
sio:SIO_000628
miriam-gene:5669
,
lld:C2678504
;
a
sio:SIO_001121
.
}
dgn-np:NP516494.RA1HlTc0c0EnqB0xK5nBP_5JJYKhGWxLLNx2ZfVzrqJow130_provenance
{
dgn-np:NP516494.RA1HlTc0c0EnqB0xK5nBP_5JJYKhGWxLLNx2ZfVzrqJow130_assertion
dcterms:description
"[Genetic factors play an important role in the pathogenesis of osteoporosis, and recent studies have shown that a polymorphic Sp1 binding site in collagen type I alpha1 (COLIA1) gene is associated with bone mass and vertebral fractures in women from the U.K. Information on the predictive value of the COLIA1 Sp1 polymorphism in other populations is limited, however, and no studies have yet been performed in osteoporotic males.]. 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:9738510
;
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:NP516494.RA1HlTc0c0EnqB0xK5nBP_5JJYKhGWxLLNx2ZfVzrqJow130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:07+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" .
}