@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP782118.RAjVVbmQ7sxHOqJeVge9XrcC1HW51TFWAhbdSQXJOPy2s
> .
@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:NP782118.RAjVVbmQ7sxHOqJeVge9XrcC1HW51TFWAhbdSQXJOPy2s130_head
{
this:
np:hasAssertion
dgn-np:NP782118.RAjVVbmQ7sxHOqJeVge9XrcC1HW51TFWAhbdSQXJOPy2s130_assertion
;
np:hasProvenance
dgn-np:NP782118.RAjVVbmQ7sxHOqJeVge9XrcC1HW51TFWAhbdSQXJOPy2s130_provenance
;
np:hasPublicationInfo
dgn-np:NP782118.RAjVVbmQ7sxHOqJeVge9XrcC1HW51TFWAhbdSQXJOPy2s130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP782118.RAjVVbmQ7sxHOqJeVge9XrcC1HW51TFWAhbdSQXJOPy2s130_assertion
a
np:Assertion
.
dgn-np:NP782118.RAjVVbmQ7sxHOqJeVge9XrcC1HW51TFWAhbdSQXJOPy2s130_provenance
a
np:Provenance
.
dgn-np:NP782118.RAjVVbmQ7sxHOqJeVge9XrcC1HW51TFWAhbdSQXJOPy2s130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP782118.RAjVVbmQ7sxHOqJeVge9XrcC1HW51TFWAhbdSQXJOPy2s130_assertion
{
miriam-gene:50964
a
ncit:C16612
.
lld:C2678504
a
ncit:C7057
.
dgn-gda:DGNf055f7be2b4ddadbf03c8cc26e2bc20b
sio:SIO_000628
miriam-gene:50964
,
lld:C2678504
;
a
sio:SIO_001121
.
}
dgn-np:NP782118.RAjVVbmQ7sxHOqJeVge9XrcC1HW51TFWAhbdSQXJOPy2s130_provenance
{
dgn-np:NP782118.RAjVVbmQ7sxHOqJeVge9XrcC1HW51TFWAhbdSQXJOPy2s130_assertion
dcterms:description
"[enhanced mRNA expression of known osteoporosis-associated genes (LRP5, RUNX2, COL1A1) and of genes involved in osteoclastogenesis (CSF1, PTH1R), but most notably of genes coding for inhibitors of WNT and BMP signaling, such as Sclerostin and MAB21L2.]. 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:23028809
;
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:NP782118.RAjVVbmQ7sxHOqJeVge9XrcC1HW51TFWAhbdSQXJOPy2s130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:54+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" .
}