@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP782195.RAZUFpFn1uEq34y5aGUlZrLJTDcgnPp4YYCYyHJ-Ysx6U
> .
@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:NP782195.RAZUFpFn1uEq34y5aGUlZrLJTDcgnPp4YYCYyHJ-Ysx6U130_head
{
this:
np:hasAssertion
dgn-np:NP782195.RAZUFpFn1uEq34y5aGUlZrLJTDcgnPp4YYCYyHJ-Ysx6U130_assertion
;
np:hasProvenance
dgn-np:NP782195.RAZUFpFn1uEq34y5aGUlZrLJTDcgnPp4YYCYyHJ-Ysx6U130_provenance
;
np:hasPublicationInfo
dgn-np:NP782195.RAZUFpFn1uEq34y5aGUlZrLJTDcgnPp4YYCYyHJ-Ysx6U130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP782195.RAZUFpFn1uEq34y5aGUlZrLJTDcgnPp4YYCYyHJ-Ysx6U130_assertion
a
np:Assertion
.
dgn-np:NP782195.RAZUFpFn1uEq34y5aGUlZrLJTDcgnPp4YYCYyHJ-Ysx6U130_provenance
a
np:Provenance
.
dgn-np:NP782195.RAZUFpFn1uEq34y5aGUlZrLJTDcgnPp4YYCYyHJ-Ysx6U130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP782195.RAZUFpFn1uEq34y5aGUlZrLJTDcgnPp4YYCYyHJ-Ysx6U130_assertion
{
miriam-gene:4982
a
ncit:C16612
.
lld:C0268414
a
ncit:C7057
.
dgn-gda:DGN49d3a30e6cb0592a10faff0a76e89958
sio:SIO_000628
miriam-gene:4982
,
lld:C0268414
;
a
sio:SIO_001121
.
}
dgn-np:NP782195.RAZUFpFn1uEq34y5aGUlZrLJTDcgnPp4YYCYyHJ-Ysx6U130_provenance
{
dgn-np:NP782195.RAZUFpFn1uEq34y5aGUlZrLJTDcgnPp4YYCYyHJ-Ysx6U130_assertion
dcterms:description
"[Because our patient shared some features in common with juvenile Paget disease, we thought that mutational analysis of TNFRSF11B was indicated, even though our patient had some manifestations not found in juvenile Paget 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:17001672
;
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:NP782195.RAZUFpFn1uEq34y5aGUlZrLJTDcgnPp4YYCYyHJ-Ysx6U130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:54+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" .
}