@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP765482.RAJg6P3LDD2b2gO41-k4rkgeNqzEEd5_gacrZsPOo4aW4
> .
@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:NP765482.RAJg6P3LDD2b2gO41-k4rkgeNqzEEd5_gacrZsPOo4aW4130_head
{
this:
np:hasAssertion
dgn-np:NP765482.RAJg6P3LDD2b2gO41-k4rkgeNqzEEd5_gacrZsPOo4aW4130_assertion
;
np:hasProvenance
dgn-np:NP765482.RAJg6P3LDD2b2gO41-k4rkgeNqzEEd5_gacrZsPOo4aW4130_provenance
;
np:hasPublicationInfo
dgn-np:NP765482.RAJg6P3LDD2b2gO41-k4rkgeNqzEEd5_gacrZsPOo4aW4130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP765482.RAJg6P3LDD2b2gO41-k4rkgeNqzEEd5_gacrZsPOo4aW4130_assertion
a
np:Assertion
.
dgn-np:NP765482.RAJg6P3LDD2b2gO41-k4rkgeNqzEEd5_gacrZsPOo4aW4130_provenance
a
np:Provenance
.
dgn-np:NP765482.RAJg6P3LDD2b2gO41-k4rkgeNqzEEd5_gacrZsPOo4aW4130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP765482.RAJg6P3LDD2b2gO41-k4rkgeNqzEEd5_gacrZsPOo4aW4130_assertion
{
miriam-gene:4982
a
ncit:C16612
.
lld:C0268414
a
ncit:C7057
.
dgn-gda:DGNe90853bc4dc917c9e37b6a6b299752b2
sio:SIO_000628
miriam-gene:4982
,
lld:C0268414
;
a
sio:SIO_001121
.
}
dgn-np:NP765482.RAJg6P3LDD2b2gO41-k4rkgeNqzEEd5_gacrZsPOo4aW4130_provenance
{
dgn-np:NP765482.RAJg6P3LDD2b2gO41-k4rkgeNqzEEd5_gacrZsPOo4aW4130_assertion
dcterms:description
"[Genetic factors are important in the pathogenesis of PDB, and studies have shown that inactivating mutations of the TNFRSF11B gene, encoding osteoprotegerin (OPG), cause the rare syndrome of juvenile 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:15312251
;
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:NP765482.RAJg6P3LDD2b2gO41-k4rkgeNqzEEd5_gacrZsPOo4aW4130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:43+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: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" .
}