@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP191128.RATwoEWwAuUQ4f23F6IiBV9V2bnk9-f05PhUqZ6oBpop0
> .
@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:NP191128.RATwoEWwAuUQ4f23F6IiBV9V2bnk9-f05PhUqZ6oBpop0130_head
{
this:
np:hasAssertion
dgn-np:NP191128.RATwoEWwAuUQ4f23F6IiBV9V2bnk9-f05PhUqZ6oBpop0130_assertion
;
np:hasProvenance
dgn-np:NP191128.RATwoEWwAuUQ4f23F6IiBV9V2bnk9-f05PhUqZ6oBpop0130_provenance
;
np:hasPublicationInfo
dgn-np:NP191128.RATwoEWwAuUQ4f23F6IiBV9V2bnk9-f05PhUqZ6oBpop0130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP191128.RATwoEWwAuUQ4f23F6IiBV9V2bnk9-f05PhUqZ6oBpop0130_assertion
a
np:Assertion
.
dgn-np:NP191128.RATwoEWwAuUQ4f23F6IiBV9V2bnk9-f05PhUqZ6oBpop0130_provenance
a
np:Provenance
.
dgn-np:NP191128.RATwoEWwAuUQ4f23F6IiBV9V2bnk9-f05PhUqZ6oBpop0130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP191128.RATwoEWwAuUQ4f23F6IiBV9V2bnk9-f05PhUqZ6oBpop0130_assertion
{
miriam-gene:2271
a
ncit:C16612
.
lld:C0002895
a
ncit:C7057
.
dgn-gda:DGN639442439c8fe2299911c0a5a5661f54
sio:SIO_000628
miriam-gene:2271
,
lld:C0002895
;
a
sio:SIO_001121
.
}
dgn-np:NP191128.RATwoEWwAuUQ4f23F6IiBV9V2bnk9-f05PhUqZ6oBpop0130_provenance
{
dgn-np:NP191128.RATwoEWwAuUQ4f23F6IiBV9V2bnk9-f05PhUqZ6oBpop0130_assertion
dcterms:description
"[Generalized cellular hypoxia (in sickle cell disease) or pseudohypoxia (in tumors with fumarate hydratase and von Hippel-Lindau mutations or epigenetic silencing) may act alone or in concert at the level of medullary tubular epithelium to promote development of this rare type of renal carcinoma, which could then be genetically reclassified as either fumarate hydratase-associated renal carcinomas or high-grade clear cell renal cell carcinomas.]. 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:21733559
;
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:NP191128.RATwoEWwAuUQ4f23F6IiBV9V2bnk9-f05PhUqZ6oBpop0130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:45+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" .
}