@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP956264.RACK4d1WDBpnx3OXp4-Em-LYKd7LNH_3_CnqjnGpj8B-g
> .
@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/v3.0.0/void/
> .
dgn-np:NP956264.RACK4d1WDBpnx3OXp4-Em-LYKd7LNH_3_CnqjnGpj8B-g130_head
{
this:
np:hasAssertion
dgn-np:NP956264.RACK4d1WDBpnx3OXp4-Em-LYKd7LNH_3_CnqjnGpj8B-g130_assertion
;
np:hasProvenance
dgn-np:NP956264.RACK4d1WDBpnx3OXp4-Em-LYKd7LNH_3_CnqjnGpj8B-g130_provenance
;
np:hasPublicationInfo
dgn-np:NP956264.RACK4d1WDBpnx3OXp4-Em-LYKd7LNH_3_CnqjnGpj8B-g130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP956264.RACK4d1WDBpnx3OXp4-Em-LYKd7LNH_3_CnqjnGpj8B-g130_assertion
a
np:Assertion
.
dgn-np:NP956264.RACK4d1WDBpnx3OXp4-Em-LYKd7LNH_3_CnqjnGpj8B-g130_provenance
a
np:Provenance
.
dgn-np:NP956264.RACK4d1WDBpnx3OXp4-Em-LYKd7LNH_3_CnqjnGpj8B-g130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP956264.RACK4d1WDBpnx3OXp4-Em-LYKd7LNH_3_CnqjnGpj8B-g130_assertion
{
miriam-gene:84447
a
ncit:C16612
.
lld:C0007134
a
ncit:C7057
.
dgn-gda:DGN40d88a8bc1bed6543213c1bbd7f14412
sio:SIO_000628
miriam-gene:84447
,
lld:C0007134
;
a
sio:SIO_001121
.
}
dgn-np:NP956264.RACK4d1WDBpnx3OXp4-Em-LYKd7LNH_3_CnqjnGpj8B-g130_provenance
{
dgn-np:NP956264.RACK4d1WDBpnx3OXp4-Em-LYKd7LNH_3_CnqjnGpj8B-g130_assertion
dcterms:description
"[Based on these results and those reported in the literature, we conclude that loss of der(3) and subsequent VHL gene mutation may represent critical steps in the development of renal cell cancers in persons carrying the chromosome 3 translocation.]. 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:11284032
;
prov:wasDerivedFrom
dgn-void:befree-20150227
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-20150227
pav:importedOn
"2015-02-27"^^
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:NP956264.RACK4d1WDBpnx3OXp4-Em-LYKd7LNH_3_CnqjnGpj8B-g130_publicationInfo
{
this:
dcterms:created
"2015-08-25T14:47:24+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
"v3.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v3.0.0" .
}