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http://rdf.disgenet.org/nanopublications.trig#NP798877.RANFzyGcU8hVJyGRSxLi3Y1kJSbl7g4mlLiHXqVVG2TWE
> .
@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#
> .
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http://rdf.disgenet.org/v2.1.0/void.ttl#
> .
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{
this:
np:hasAssertion
dgn-np:NP798877.RANFzyGcU8hVJyGRSxLi3Y1kJSbl7g4mlLiHXqVVG2TWE130_assertion
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np:hasProvenance
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np:hasPublicationInfo
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a
np:Nanopublication
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dgn-np:NP798877.RANFzyGcU8hVJyGRSxLi3Y1kJSbl7g4mlLiHXqVVG2TWE130_assertion
a
np:Assertion
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dgn-np:NP798877.RANFzyGcU8hVJyGRSxLi3Y1kJSbl7g4mlLiHXqVVG2TWE130_provenance
a
np:Provenance
.
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np:PublicationInfo
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{
miriam-gene:2272
a
ncit:C16612
.
lld:C0280100
a
ncit:C7057
.
dgn-gda:DGN30c97280d721a4e3eefa973de93d1937
sio:SIO_000628
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,
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;
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.
}
dgn-np:NP798877.RANFzyGcU8hVJyGRSxLi3Y1kJSbl7g4mlLiHXqVVG2TWE130_provenance
{
dgn-np:NP798877.RANFzyGcU8hVJyGRSxLi3Y1kJSbl7g4mlLiHXqVVG2TWE130_assertion
dcterms:description
"[To evaluate the loss of C3CER1 in various human tumor types, we conducted loss of heterozygosity (LOH) analysis of 576 human solid tumors from 10 different tissues and compared the frequency of deletion in the C3CER1 area to that in two other regions on 3p: the FHIT/FRA3B region, at 3p14.2, and the VHL region, at 3p25.3.]. 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:15334546
;
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 .
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dgn-np:NP798877.RANFzyGcU8hVJyGRSxLi3Y1kJSbl7g4mlLiHXqVVG2TWE130_publicationInfo
{
this:
dcterms:created
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xsd:dateTime
;
dcterms:rights
<
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> ;
dcterms:rightsHolder
dgn-void:IBIGroup
;
dcterms:subject
sio:SIO_000983
;
prv:usedData
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> , <
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> , <
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> , <
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> ;
pav:createdBy
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> ;
pav:version
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}