@prefix dct: <
http://purl.org/dc/terms/
> .
@prefix orcid: <
http://orcid.org/
> .
@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP358195.RAA9YY3U7o5UZemu5s3Zrub4qGHCmxCJPmqIs-oUazaSI
> .
@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 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:NP358195.RAA9YY3U7o5UZemu5s3Zrub4qGHCmxCJPmqIs-oUazaSI130_head
{
this:
np:hasAssertion
dgn-np:NP358195.RAA9YY3U7o5UZemu5s3Zrub4qGHCmxCJPmqIs-oUazaSI130_assertion
;
np:hasProvenance
dgn-np:NP358195.RAA9YY3U7o5UZemu5s3Zrub4qGHCmxCJPmqIs-oUazaSI130_provenance
;
np:hasPublicationInfo
dgn-np:NP358195.RAA9YY3U7o5UZemu5s3Zrub4qGHCmxCJPmqIs-oUazaSI130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP358195.RAA9YY3U7o5UZemu5s3Zrub4qGHCmxCJPmqIs-oUazaSI130_assertion
a
np:Assertion
.
dgn-np:NP358195.RAA9YY3U7o5UZemu5s3Zrub4qGHCmxCJPmqIs-oUazaSI130_provenance
a
np:Provenance
.
dgn-np:NP358195.RAA9YY3U7o5UZemu5s3Zrub4qGHCmxCJPmqIs-oUazaSI130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP358195.RAA9YY3U7o5UZemu5s3Zrub4qGHCmxCJPmqIs-oUazaSI130_assertion
{
miriam-gene:8878
a
ncit:C16612
.
lld:C1368019
a
ncit:C7057
.
dgn-gda:DGNce413fd24b69b03cdf9aad18f87be14b
sio:SIO_000628
miriam-gene:8878
,
lld:C1368019
;
a
sio:SIO_001121
.
}
dgn-np:NP358195.RAA9YY3U7o5UZemu5s3Zrub4qGHCmxCJPmqIs-oUazaSI130_provenance
{
dgn-np:NP358195.RAA9YY3U7o5UZemu5s3Zrub4qGHCmxCJPmqIs-oUazaSI130_assertion
dct:description
"[New insights from the biology of adolescent osteosarcomas, VCP and SQSTM1 mutations now defined in patients with Paget's disease, and emerging evidence that stromal lesions are present in patients with Paget's disease are changing the way we think about the pathogenesis of PDB and the rare complication of pagetic osteosarcomas.]. 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:17229010
;
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:NP358195.RAA9YY3U7o5UZemu5s3Zrub4qGHCmxCJPmqIs-oUazaSI130_publicationInfo
{
this:
dct:created
"2014-10-02T12:35:30+02:00"^^
xsd:dateTime
;
dct:rights
<
http://opendatacommons.org/licenses/odbl/1.0/
> ;
dct:rightsHolder
dgn-void:IBIGroup
;
dct:subject
sio:SIO_000983
;
prv:usedData
dgn-void:disgenetrdf
;
pav:authoredBy
orcid:0000-0001-5999-6269
,
orcid:0000-0002-7534-7661
,
orcid:0000-0002-9383-528X
,
orcid:0000-0003-0169-8159
,
orcid:0000-0003-1244-7654
;
pav:createdBy
orcid:0000-0003-0169-8159
;
pav:version
"v2.1.0.0" .
dgn-void:disgenetrdf
pav:version
"v2.1.0" .
}