@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP293992.RA1YiZTVbid5MvCDCqOqaHU7BC7iLTiE-E20Q0W7_ivCA
> .
@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/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@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/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v4.0.0/void/
> .
dgn-np:NP293992.RA1YiZTVbid5MvCDCqOqaHU7BC7iLTiE-E20Q0W7_ivCA130_head
{
this:
np:hasAssertion
dgn-np:NP293992.RA1YiZTVbid5MvCDCqOqaHU7BC7iLTiE-E20Q0W7_ivCA130_assertion
;
np:hasProvenance
dgn-np:NP293992.RA1YiZTVbid5MvCDCqOqaHU7BC7iLTiE-E20Q0W7_ivCA130_provenance
;
np:hasPublicationInfo
dgn-np:NP293992.RA1YiZTVbid5MvCDCqOqaHU7BC7iLTiE-E20Q0W7_ivCA130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP293992.RA1YiZTVbid5MvCDCqOqaHU7BC7iLTiE-E20Q0W7_ivCA130_assertion
a
np:Assertion
.
dgn-np:NP293992.RA1YiZTVbid5MvCDCqOqaHU7BC7iLTiE-E20Q0W7_ivCA130_provenance
a
np:Provenance
.
dgn-np:NP293992.RA1YiZTVbid5MvCDCqOqaHU7BC7iLTiE-E20Q0W7_ivCA130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP293992.RA1YiZTVbid5MvCDCqOqaHU7BC7iLTiE-E20Q0W7_ivCA130_assertion
{
miriam-gene:7428
a
ncit:C16612
.
lld:C0740457
a
ncit:C7057
.
dgn-gda:DGN531a1730d553ac12e3971c6901102f0e
sio:SIO_000628
miriam-gene:7428
,
lld:C0740457
;
a
sio:SIO_001121
.
}
dgn-np:NP293992.RA1YiZTVbid5MvCDCqOqaHU7BC7iLTiE-E20Q0W7_ivCA130_provenance
{
dgn-np:NP293992.RA1YiZTVbid5MvCDCqOqaHU7BC7iLTiE-E20Q0W7_ivCA130_assertion
dcterms:description
"[The most common chromosome abnormality found in this tumor is loss of heterozygosity (LOH) on the short arm of chromosome 3, which suggests that there must be one or more tumor suppressor genes between 3p14 and 3p21 near the VHL gene which play a relevant role in renal cancer development.]. 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:10971171
;
prov:wasDerivedFrom
dgn-void:befree-2016
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-2016
pav:importedOn
"2016-02-19"^^
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:NP293992.RA1YiZTVbid5MvCDCqOqaHU7BC7iLTiE-E20Q0W7_ivCA130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:43:59+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:disgenetv3.0rdf
;
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
"v4.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v4.0.0" .
}