@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP521218.RA_WCmFch_qza4Ton88cdMiYUbeBP4pIf8Vjt-MwuVhF4
> .
@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:NP521218.RA_WCmFch_qza4Ton88cdMiYUbeBP4pIf8Vjt-MwuVhF4130_head
{
this:
np:hasAssertion
dgn-np:NP521218.RA_WCmFch_qza4Ton88cdMiYUbeBP4pIf8Vjt-MwuVhF4130_assertion
;
np:hasProvenance
dgn-np:NP521218.RA_WCmFch_qza4Ton88cdMiYUbeBP4pIf8Vjt-MwuVhF4130_provenance
;
np:hasPublicationInfo
dgn-np:NP521218.RA_WCmFch_qza4Ton88cdMiYUbeBP4pIf8Vjt-MwuVhF4130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP521218.RA_WCmFch_qza4Ton88cdMiYUbeBP4pIf8Vjt-MwuVhF4130_assertion
a
np:Assertion
.
dgn-np:NP521218.RA_WCmFch_qza4Ton88cdMiYUbeBP4pIf8Vjt-MwuVhF4130_provenance
a
np:Provenance
.
dgn-np:NP521218.RA_WCmFch_qza4Ton88cdMiYUbeBP4pIf8Vjt-MwuVhF4130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP521218.RA_WCmFch_qza4Ton88cdMiYUbeBP4pIf8Vjt-MwuVhF4130_assertion
{
miriam-gene:8600
a
ncit:C16612
.
lld:C0029401
a
ncit:C7057
.
dgn-gda:DGNc3f6db3461e4f795771ca918f801079c
sio:SIO_000628
miriam-gene:8600
,
lld:C0029401
;
a
sio:SIO_001121
.
}
dgn-np:NP521218.RA_WCmFch_qza4Ton88cdMiYUbeBP4pIf8Vjt-MwuVhF4130_provenance
{
dgn-np:NP521218.RA_WCmFch_qza4Ton88cdMiYUbeBP4pIf8Vjt-MwuVhF4130_assertion
dcterms:description
"[These data suggest that the combination of enhanced expression of RANKL in affected bones and increased RANKL sensitivity of pagetic OCL precursors may contribute to the elevated numbers of OCLs in Paget's disease.]. 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:10862799
;
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:NP521218.RA_WCmFch_qza4Ton88cdMiYUbeBP4pIf8Vjt-MwuVhF4130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:10+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" .
}