@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP527576.RAHOsto9ligM6_zI1VLWAzlHcrZ3csX7wk2Vvb_M6mAKE
> .
@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:NP527576.RAHOsto9ligM6_zI1VLWAzlHcrZ3csX7wk2Vvb_M6mAKE130_head
{
this:
np:hasAssertion
dgn-np:NP527576.RAHOsto9ligM6_zI1VLWAzlHcrZ3csX7wk2Vvb_M6mAKE130_assertion
;
np:hasProvenance
dgn-np:NP527576.RAHOsto9ligM6_zI1VLWAzlHcrZ3csX7wk2Vvb_M6mAKE130_provenance
;
np:hasPublicationInfo
dgn-np:NP527576.RAHOsto9ligM6_zI1VLWAzlHcrZ3csX7wk2Vvb_M6mAKE130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP527576.RAHOsto9ligM6_zI1VLWAzlHcrZ3csX7wk2Vvb_M6mAKE130_assertion
a
np:Assertion
.
dgn-np:NP527576.RAHOsto9ligM6_zI1VLWAzlHcrZ3csX7wk2Vvb_M6mAKE130_provenance
a
np:Provenance
.
dgn-np:NP527576.RAHOsto9ligM6_zI1VLWAzlHcrZ3csX7wk2Vvb_M6mAKE130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP527576.RAHOsto9ligM6_zI1VLWAzlHcrZ3csX7wk2Vvb_M6mAKE130_assertion
{
miriam-gene:1435
a
ncit:C16612
.
lld:C2678504
a
ncit:C7057
.
dgn-gda:DGN6bc78c79e3055d4f93bdb86e2bb76d06
sio:SIO_000628
miriam-gene:1435
,
lld:C2678504
;
a
sio:SIO_001121
.
}
dgn-np:NP527576.RAHOsto9ligM6_zI1VLWAzlHcrZ3csX7wk2Vvb_M6mAKE130_provenance
{
dgn-np:NP527576.RAHOsto9ligM6_zI1VLWAzlHcrZ3csX7wk2Vvb_M6mAKE130_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:NP527576.RAHOsto9ligM6_zI1VLWAzlHcrZ3csX7wk2Vvb_M6mAKE130_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" .
}