@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP526986.RA4wcJyNh0NCkzwVMvpxn4p7HaSOzBGqO0LdvobSNOl2o
> .
@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:NP526986.RA4wcJyNh0NCkzwVMvpxn4p7HaSOzBGqO0LdvobSNOl2o130_head
{
this:
np:hasAssertion
dgn-np:NP526986.RA4wcJyNh0NCkzwVMvpxn4p7HaSOzBGqO0LdvobSNOl2o130_assertion
;
np:hasProvenance
dgn-np:NP526986.RA4wcJyNh0NCkzwVMvpxn4p7HaSOzBGqO0LdvobSNOl2o130_provenance
;
np:hasPublicationInfo
dgn-np:NP526986.RA4wcJyNh0NCkzwVMvpxn4p7HaSOzBGqO0LdvobSNOl2o130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP526986.RA4wcJyNh0NCkzwVMvpxn4p7HaSOzBGqO0LdvobSNOl2o130_assertion
a
np:Assertion
.
dgn-np:NP526986.RA4wcJyNh0NCkzwVMvpxn4p7HaSOzBGqO0LdvobSNOl2o130_provenance
a
np:Provenance
.
dgn-np:NP526986.RA4wcJyNh0NCkzwVMvpxn4p7HaSOzBGqO0LdvobSNOl2o130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP526986.RA4wcJyNh0NCkzwVMvpxn4p7HaSOzBGqO0LdvobSNOl2o130_assertion
{
miriam-gene:199699
a
ncit:C16612
.
lld:C2678504
a
ncit:C7057
.
dgn-gda:DGN617de338871dbe1f594c7d654f7dccbd
sio:SIO_000628
miriam-gene:199699
,
lld:C2678504
;
a
sio:SIO_001121
.
}
dgn-np:NP526986.RA4wcJyNh0NCkzwVMvpxn4p7HaSOzBGqO0LdvobSNOl2o130_provenance
{
dgn-np:NP526986.RA4wcJyNh0NCkzwVMvpxn4p7HaSOzBGqO0LdvobSNOl2o130_assertion
dcterms:description
"[While the mechanisms that underlie this association remain to be defined, the COLIA1 Sp1 polymorphism appears to be an important marker for low bone mass and vertebral fracture, raising the possibility that genotyping at this site may be of value in identifying women who are at risk of osteoporosis.]. 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:8841196
;
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:NP526986.RA4wcJyNh0NCkzwVMvpxn4p7HaSOzBGqO0LdvobSNOl2o130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:16+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" .
}