@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP267529.RA9sY1Gnws0q1aom1MTpoMRSRkxVcrtpOrh6TWT9IBR_A
> .
@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:NP267529.RA9sY1Gnws0q1aom1MTpoMRSRkxVcrtpOrh6TWT9IBR_A130_head
{
this:
np:hasAssertion
dgn-np:NP267529.RA9sY1Gnws0q1aom1MTpoMRSRkxVcrtpOrh6TWT9IBR_A130_assertion
;
np:hasProvenance
dgn-np:NP267529.RA9sY1Gnws0q1aom1MTpoMRSRkxVcrtpOrh6TWT9IBR_A130_provenance
;
np:hasPublicationInfo
dgn-np:NP267529.RA9sY1Gnws0q1aom1MTpoMRSRkxVcrtpOrh6TWT9IBR_A130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP267529.RA9sY1Gnws0q1aom1MTpoMRSRkxVcrtpOrh6TWT9IBR_A130_assertion
a
np:Assertion
.
dgn-np:NP267529.RA9sY1Gnws0q1aom1MTpoMRSRkxVcrtpOrh6TWT9IBR_A130_provenance
a
np:Provenance
.
dgn-np:NP267529.RA9sY1Gnws0q1aom1MTpoMRSRkxVcrtpOrh6TWT9IBR_A130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP267529.RA9sY1Gnws0q1aom1MTpoMRSRkxVcrtpOrh6TWT9IBR_A130_assertion
{
miriam-gene:690
a
ncit:C16612
.
lld:C0029401
a
ncit:C7057
.
dgn-gda:DGN816a145bb2646a167b8a6f7042b13299
sio:SIO_000628
miriam-gene:690
,
lld:C0029401
;
a
sio:SIO_001121
.
}
dgn-np:NP267529.RA9sY1Gnws0q1aom1MTpoMRSRkxVcrtpOrh6TWT9IBR_A130_provenance
{
dgn-np:NP267529.RA9sY1Gnws0q1aom1MTpoMRSRkxVcrtpOrh6TWT9IBR_A130_assertion
dcterms:description
"[Although mutations in this gene have never been found in patients with typical Paget's disease of bone (PDB), there are indications that polymorphisms in TNFRSF11B might contribute to the risk of developing PDB.]. 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:17388729
;
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:NP267529.RA9sY1Gnws0q1aom1MTpoMRSRkxVcrtpOrh6TWT9IBR_A130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:29+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" .
}