@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP370938.RA6_n5ysYsTJ77bu0w9P6aZhBlaR5Y2MlHWRVFtUMpY4o
> .
@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:NP370938.RA6_n5ysYsTJ77bu0w9P6aZhBlaR5Y2MlHWRVFtUMpY4o130_head
{
this:
np:hasAssertion
dgn-np:NP370938.RA6_n5ysYsTJ77bu0w9P6aZhBlaR5Y2MlHWRVFtUMpY4o130_assertion
;
np:hasProvenance
dgn-np:NP370938.RA6_n5ysYsTJ77bu0w9P6aZhBlaR5Y2MlHWRVFtUMpY4o130_provenance
;
np:hasPublicationInfo
dgn-np:NP370938.RA6_n5ysYsTJ77bu0w9P6aZhBlaR5Y2MlHWRVFtUMpY4o130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP370938.RA6_n5ysYsTJ77bu0w9P6aZhBlaR5Y2MlHWRVFtUMpY4o130_assertion
a
np:Assertion
.
dgn-np:NP370938.RA6_n5ysYsTJ77bu0w9P6aZhBlaR5Y2MlHWRVFtUMpY4o130_provenance
a
np:Provenance
.
dgn-np:NP370938.RA6_n5ysYsTJ77bu0w9P6aZhBlaR5Y2MlHWRVFtUMpY4o130_publicationInfo
a
np:PublicationInfo
.
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dgn-np:NP370938.RA6_n5ysYsTJ77bu0w9P6aZhBlaR5Y2MlHWRVFtUMpY4o130_assertion
{
miriam-gene:7157
a
ncit:C16612
.
lld:C0278701
a
ncit:C7057
.
dgn-gda:DGN83cabed2e998d1515c1fdac868fa06e9
sio:SIO_000628
miriam-gene:7157
,
lld:C0278701
;
a
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.
}
dgn-np:NP370938.RA6_n5ysYsTJ77bu0w9P6aZhBlaR5Y2MlHWRVFtUMpY4o130_provenance
{
dgn-np:NP370938.RA6_n5ysYsTJ77bu0w9P6aZhBlaR5Y2MlHWRVFtUMpY4o130_assertion
dcterms:description
"[Using a fluorescence in situ hybridization technique, we investigated the occurrence of aneuploidies of chromosomes 3, 7, 8, 9, and 17, TP53 gene deletion, and expression of p53 in 21 intestinal metaplasia (IM) samples from cancer-free patients and in 20 gastric adenocarcinoma samples.]. 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:15350302
;
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:NP370938.RA6_n5ysYsTJ77bu0w9P6aZhBlaR5Y2MlHWRVFtUMpY4o130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:37+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
<
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> , <
http://orcid.org/0000-0002-7534-7661
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> , <
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> , <
http://orcid.org/0000-0003-1244-7654
> ;
pav:createdBy
<
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> ;
pav:version
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dgn-void:disgenetrdf
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}