@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP798989.RAobb4ii6N9WOBNXIE329kTim52U0ccn3ROHtFRZ2IyyM
> .
@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/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@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/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v3.0.0/void/
> .
dgn-np:NP798989.RAobb4ii6N9WOBNXIE329kTim52U0ccn3ROHtFRZ2IyyM130_head
{
this:
np:hasAssertion
dgn-np:NP798989.RAobb4ii6N9WOBNXIE329kTim52U0ccn3ROHtFRZ2IyyM130_assertion
;
np:hasProvenance
dgn-np:NP798989.RAobb4ii6N9WOBNXIE329kTim52U0ccn3ROHtFRZ2IyyM130_provenance
;
np:hasPublicationInfo
dgn-np:NP798989.RAobb4ii6N9WOBNXIE329kTim52U0ccn3ROHtFRZ2IyyM130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP798989.RAobb4ii6N9WOBNXIE329kTim52U0ccn3ROHtFRZ2IyyM130_assertion
a
np:Assertion
.
dgn-np:NP798989.RAobb4ii6N9WOBNXIE329kTim52U0ccn3ROHtFRZ2IyyM130_provenance
a
np:Provenance
.
dgn-np:NP798989.RAobb4ii6N9WOBNXIE329kTim52U0ccn3ROHtFRZ2IyyM130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP798989.RAobb4ii6N9WOBNXIE329kTim52U0ccn3ROHtFRZ2IyyM130_assertion
{
miriam-gene:8600
a
ncit:C16612
.
lld:C0432292
a
ncit:C7057
.
dgn-gda:DGN1bdc1f5dc0a612d9720eff4876c75264
sio:SIO_000628
miriam-gene:8600
,
lld:C0432292
;
a
sio:SIO_001121
.
}
dgn-np:NP798989.RAobb4ii6N9WOBNXIE329kTim52U0ccn3ROHtFRZ2IyyM130_provenance
{
dgn-np:NP798989.RAobb4ii6N9WOBNXIE329kTim52U0ccn3ROHtFRZ2IyyM130_assertion
dcterms:description
"[Whilst no mutations in the RANKL gene have yet been identified in human disease, mutations that result in enhanced RANK signalling through inactivation of OPG or activation of RANK are associated with Juvenile Paget's disease and familial expansile osteolysis, respectively.]. 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:17174136
;
prov:wasDerivedFrom
dgn-void:befree-20150227
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-20150227
pav:importedOn
"2015-02-27"^^
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:NP798989.RAobb4ii6N9WOBNXIE329kTim52U0ccn3ROHtFRZ2IyyM130_publicationInfo
{
this:
dcterms:created
"2015-08-25T14:45:43+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:disgenetv3.0rdf
;
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
"v3.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v3.0.0" .
}