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http://rdf.disgenet.org/resource/nanopub/NP345551.RAUItf-Na9WVj2SIeoRuMYXk4_VusVgsEL2BVuCNt10YA
> .
@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/
> .
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{
this:
np:hasAssertion
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;
np:hasProvenance
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np:hasPublicationInfo
dgn-np:NP345551.RAUItf-Na9WVj2SIeoRuMYXk4_VusVgsEL2BVuCNt10YA130_publicationInfo
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a
np:Nanopublication
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a
np:Assertion
.
dgn-np:NP345551.RAUItf-Na9WVj2SIeoRuMYXk4_VusVgsEL2BVuCNt10YA130_provenance
a
np:Provenance
.
dgn-np:NP345551.RAUItf-Na9WVj2SIeoRuMYXk4_VusVgsEL2BVuCNt10YA130_publicationInfo
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{
miriam-gene:7428
a
ncit:C16612
.
lld:C1333955
a
ncit:C7057
.
dgn-gda:DGN29a5c09e134bc3fbce3a23bde2aa93a8
sio:SIO_000628
miriam-gene:7428
,
lld:C1333955
;
a
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.
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dgn-np:NP345551.RAUItf-Na9WVj2SIeoRuMYXk4_VusVgsEL2BVuCNt10YA130_provenance
{
dgn-np:NP345551.RAUItf-Na9WVj2SIeoRuMYXk4_VusVgsEL2BVuCNt10YA130_assertion
dcterms:description
"[To investigate the nature of the second genetic hit in this patient population, we analysed two renal cell carcinomas and one CNS hemangioblastoma from three unrelated patients for genetic changes of the second copy of the VHL gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ;
wi:evidence
dgn-void:source_evidence_literature
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sio:SIO_000772
miriam-pubmed:11850836
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prov:wasDerivedFrom
dgn-void:befree-2016
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prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-2016
pav:importedOn
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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 .
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dgn-np:NP345551.RAUItf-Na9WVj2SIeoRuMYXk4_VusVgsEL2BVuCNt10YA130_publicationInfo
{
this:
dcterms:created
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xsd:dateTime
;
dcterms:rights
<
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> ;
dcterms:rightsHolder
dgn-void:IBIGroup
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dcterms:subject
sio:SIO_000983
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> , <
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> , <
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pav:createdBy
<
http://orcid.org/0000-0003-0169-8159
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