@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP46700.RA77FO2FViH4wvYNy9pMsTbnAiok5cyCo4DLvDr5veXVM
> .
@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:NP46700.RA77FO2FViH4wvYNy9pMsTbnAiok5cyCo4DLvDr5veXVM130_head
{
this:
np:hasAssertion
dgn-np:NP46700.RA77FO2FViH4wvYNy9pMsTbnAiok5cyCo4DLvDr5veXVM130_assertion
;
np:hasProvenance
dgn-np:NP46700.RA77FO2FViH4wvYNy9pMsTbnAiok5cyCo4DLvDr5veXVM130_provenance
;
np:hasPublicationInfo
dgn-np:NP46700.RA77FO2FViH4wvYNy9pMsTbnAiok5cyCo4DLvDr5veXVM130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP46700.RA77FO2FViH4wvYNy9pMsTbnAiok5cyCo4DLvDr5veXVM130_assertion
a
np:Assertion
.
dgn-np:NP46700.RA77FO2FViH4wvYNy9pMsTbnAiok5cyCo4DLvDr5veXVM130_provenance
a
np:Provenance
.
dgn-np:NP46700.RA77FO2FViH4wvYNy9pMsTbnAiok5cyCo4DLvDr5veXVM130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP46700.RA77FO2FViH4wvYNy9pMsTbnAiok5cyCo4DLvDr5veXVM130_assertion
{
miriam-gene:1277
a
ncit:C16612
.
lld:C0029453
a
ncit:C7057
.
dgn-gda:DGN8cf4a904429dfb65a6a3c8aef1dd532a
sio:SIO_000628
miriam-gene:1277
,
lld:C0029453
;
a
sio:SIO_001122
.
}
dgn-np:NP46700.RA77FO2FViH4wvYNy9pMsTbnAiok5cyCo4DLvDr5veXVM130_provenance
{
dgn-np:NP46700.RA77FO2FViH4wvYNy9pMsTbnAiok5cyCo4DLvDr5veXVM130_assertion
dcterms:description
"[We conclude that women homozygous for the Sp1 polymorphism are at significantly increased risk of excess rates of bone loss at the spine, but this effect may be nullified by the use of HRT.]. 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:11547832
;
prov:wasDerivedFrom
dgn-void:gad-20130706
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:gad-20130706
pav:importedOn
"2013-07-06"^^
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:NP46700.RA77FO2FViH4wvYNy9pMsTbnAiok5cyCo4DLvDr5veXVM130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:21+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" .
}