@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP799277.RAr1AXN1Gl6xbvEgYAaTHdFGaBJpihcsFuoaCrAktuEcQ
> .
@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:NP799277.RAr1AXN1Gl6xbvEgYAaTHdFGaBJpihcsFuoaCrAktuEcQ130_head
{
this:
np:hasAssertion
dgn-np:NP799277.RAr1AXN1Gl6xbvEgYAaTHdFGaBJpihcsFuoaCrAktuEcQ130_assertion
;
np:hasProvenance
dgn-np:NP799277.RAr1AXN1Gl6xbvEgYAaTHdFGaBJpihcsFuoaCrAktuEcQ130_provenance
;
np:hasPublicationInfo
dgn-np:NP799277.RAr1AXN1Gl6xbvEgYAaTHdFGaBJpihcsFuoaCrAktuEcQ130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP799277.RAr1AXN1Gl6xbvEgYAaTHdFGaBJpihcsFuoaCrAktuEcQ130_assertion
a
np:Assertion
.
dgn-np:NP799277.RAr1AXN1Gl6xbvEgYAaTHdFGaBJpihcsFuoaCrAktuEcQ130_provenance
a
np:Provenance
.
dgn-np:NP799277.RAr1AXN1Gl6xbvEgYAaTHdFGaBJpihcsFuoaCrAktuEcQ130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP799277.RAr1AXN1Gl6xbvEgYAaTHdFGaBJpihcsFuoaCrAktuEcQ130_assertion
{
miriam-gene:58191
a
ncit:C16612
.
lld:C0007134
a
ncit:C7057
.
dgn-gda:DGN06d75f89d942c7d99f0eb498ee6cca77
sio:SIO_000628
miriam-gene:58191
,
lld:C0007134
;
a
sio:SIO_001121
.
}
dgn-np:NP799277.RAr1AXN1Gl6xbvEgYAaTHdFGaBJpihcsFuoaCrAktuEcQ130_provenance
{
dgn-np:NP799277.RAr1AXN1Gl6xbvEgYAaTHdFGaBJpihcsFuoaCrAktuEcQ130_assertion
dcterms:description
"[Taken together, our data demonstrate that downregulation of CXCL16 plays an important role in renal cancer development and progression, and that CXCL16 in RCC is an independent prognostic marker for better patient survival.]. 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:19070478
;
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:NP799277.RAr1AXN1Gl6xbvEgYAaTHdFGaBJpihcsFuoaCrAktuEcQ130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:10+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" .
}