@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP245576.RAwrV7HhSv88Ajr3BV8P5FnBlDcALGlfnkmpecViaiDBg
> .
@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:NP245576.RAwrV7HhSv88Ajr3BV8P5FnBlDcALGlfnkmpecViaiDBg130_head
{
this:
np:hasAssertion
dgn-np:NP245576.RAwrV7HhSv88Ajr3BV8P5FnBlDcALGlfnkmpecViaiDBg130_assertion
;
np:hasProvenance
dgn-np:NP245576.RAwrV7HhSv88Ajr3BV8P5FnBlDcALGlfnkmpecViaiDBg130_provenance
;
np:hasPublicationInfo
dgn-np:NP245576.RAwrV7HhSv88Ajr3BV8P5FnBlDcALGlfnkmpecViaiDBg130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP245576.RAwrV7HhSv88Ajr3BV8P5FnBlDcALGlfnkmpecViaiDBg130_assertion
a
np:Assertion
.
dgn-np:NP245576.RAwrV7HhSv88Ajr3BV8P5FnBlDcALGlfnkmpecViaiDBg130_provenance
a
np:Provenance
.
dgn-np:NP245576.RAwrV7HhSv88Ajr3BV8P5FnBlDcALGlfnkmpecViaiDBg130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP245576.RAwrV7HhSv88Ajr3BV8P5FnBlDcALGlfnkmpecViaiDBg130_assertion
{
miriam-gene:4982
a
ncit:C16612
.
lld:C2678504
a
ncit:C7057
.
dgn-gda:DGN13a8fb89f88bf9a9f5f5a5783f127eda
sio:SIO_000628
miriam-gene:4982
,
lld:C2678504
;
a
sio:SIO_001121
.
}
dgn-np:NP245576.RAwrV7HhSv88Ajr3BV8P5FnBlDcALGlfnkmpecViaiDBg130_provenance
{
dgn-np:NP245576.RAwrV7HhSv88Ajr3BV8P5FnBlDcALGlfnkmpecViaiDBg130_assertion
dcterms:description
"[As variations in the TNFRSF11B gene could alter the susceptibility to osteoporosis, the aim of study was to investigate association of two TNFRSF11B gene polymorphisms with BMD and serum OPG concentration in 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:21411255
;
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:NP245576.RAwrV7HhSv88Ajr3BV8P5FnBlDcALGlfnkmpecViaiDBg130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:17+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" .
}