@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP374705.RArB98OiuzsOw5XpL9cSwg8hHlRdFC7yNtl4bTEn8MMQs
> .
@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:NP374705.RArB98OiuzsOw5XpL9cSwg8hHlRdFC7yNtl4bTEn8MMQs130_head
{
this:
np:hasAssertion
dgn-np:NP374705.RArB98OiuzsOw5XpL9cSwg8hHlRdFC7yNtl4bTEn8MMQs130_assertion
;
np:hasProvenance
dgn-np:NP374705.RArB98OiuzsOw5XpL9cSwg8hHlRdFC7yNtl4bTEn8MMQs130_provenance
;
np:hasPublicationInfo
dgn-np:NP374705.RArB98OiuzsOw5XpL9cSwg8hHlRdFC7yNtl4bTEn8MMQs130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP374705.RArB98OiuzsOw5XpL9cSwg8hHlRdFC7yNtl4bTEn8MMQs130_assertion
a
np:Assertion
.
dgn-np:NP374705.RArB98OiuzsOw5XpL9cSwg8hHlRdFC7yNtl4bTEn8MMQs130_provenance
a
np:Provenance
.
dgn-np:NP374705.RArB98OiuzsOw5XpL9cSwg8hHlRdFC7yNtl4bTEn8MMQs130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP374705.RArB98OiuzsOw5XpL9cSwg8hHlRdFC7yNtl4bTEn8MMQs130_assertion
{
miriam-gene:8837
a
ncit:C16612
.
lld:C0006826
a
ncit:C7057
.
dgn-gda:DGN1ca709110eeff87cfd23d6d62e5c47c2
sio:SIO_000628
miriam-gene:8837
,
lld:C0006826
;
a
sio:SIO_001121
.
}
dgn-np:NP374705.RArB98OiuzsOw5XpL9cSwg8hHlRdFC7yNtl4bTEn8MMQs130_provenance
{
dgn-np:NP374705.RArB98OiuzsOw5XpL9cSwg8hHlRdFC7yNtl4bTEn8MMQs130_assertion
dcterms:description
"[Abnormalities of various components of these pathways have been identified in human cancer including loss of FAS expression, deletion or loss of TRAIL receptor DR4, mutation of TRAIL receptor DR5, overexpression of TRAIL decoy TRID or overexpression of Fas decoy, as well as overexpression of the caspase activation inhibitor, FLIP.]. 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:12654257
;
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:NP374705.RArB98OiuzsOw5XpL9cSwg8hHlRdFC7yNtl4bTEn8MMQs130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:39+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" .
}