@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP313498.RA-oPPLkeD_E1E7qCLl__HjGoiRqX8LJXJtuoNPS0JUFA
> .
@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:NP313498.RA-oPPLkeD_E1E7qCLl__HjGoiRqX8LJXJtuoNPS0JUFA130_head
{
this:
np:hasAssertion
dgn-np:NP313498.RA-oPPLkeD_E1E7qCLl__HjGoiRqX8LJXJtuoNPS0JUFA130_assertion
;
np:hasProvenance
dgn-np:NP313498.RA-oPPLkeD_E1E7qCLl__HjGoiRqX8LJXJtuoNPS0JUFA130_provenance
;
np:hasPublicationInfo
dgn-np:NP313498.RA-oPPLkeD_E1E7qCLl__HjGoiRqX8LJXJtuoNPS0JUFA130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP313498.RA-oPPLkeD_E1E7qCLl__HjGoiRqX8LJXJtuoNPS0JUFA130_assertion
a
np:Assertion
.
dgn-np:NP313498.RA-oPPLkeD_E1E7qCLl__HjGoiRqX8LJXJtuoNPS0JUFA130_provenance
a
np:Provenance
.
dgn-np:NP313498.RA-oPPLkeD_E1E7qCLl__HjGoiRqX8LJXJtuoNPS0JUFA130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP313498.RA-oPPLkeD_E1E7qCLl__HjGoiRqX8LJXJtuoNPS0JUFA130_assertion
{
miriam-gene:7157
a
ncit:C16612
.
lld:C0003873
a
ncit:C7057
.
dgn-gda:DGNbf926748d9a90266d8fa99c6bff419ac
sio:SIO_000628
miriam-gene:7157
,
lld:C0003873
;
a
sio:SIO_001121
.
}
dgn-np:NP313498.RA-oPPLkeD_E1E7qCLl__HjGoiRqX8LJXJtuoNPS0JUFA130_provenance
{
dgn-np:NP313498.RA-oPPLkeD_E1E7qCLl__HjGoiRqX8LJXJtuoNPS0JUFA130_assertion
dcterms:description
"[The findings of the study support the hypothesis that the majority of the mutations of the p53 gene observed in RA synovium are not derived from the genome of RA synovial fibroblasts, and that the variability of the mutation pattern reflects, in part, the heterogeneity of the 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:10446856
;
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:NP313498.RA-oPPLkeD_E1E7qCLl__HjGoiRqX8LJXJtuoNPS0JUFA130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:59+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" .
}