@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP193689.RA-CA-GnuDpAOXqhtwHgOtmRqm5NK7QlAUL4mPlQ-PIBc
> .
@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:NP193689.RA-CA-GnuDpAOXqhtwHgOtmRqm5NK7QlAUL4mPlQ-PIBc130_head
{
this:
np:hasAssertion
dgn-np:NP193689.RA-CA-GnuDpAOXqhtwHgOtmRqm5NK7QlAUL4mPlQ-PIBc130_assertion
;
np:hasProvenance
dgn-np:NP193689.RA-CA-GnuDpAOXqhtwHgOtmRqm5NK7QlAUL4mPlQ-PIBc130_provenance
;
np:hasPublicationInfo
dgn-np:NP193689.RA-CA-GnuDpAOXqhtwHgOtmRqm5NK7QlAUL4mPlQ-PIBc130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP193689.RA-CA-GnuDpAOXqhtwHgOtmRqm5NK7QlAUL4mPlQ-PIBc130_assertion
a
np:Assertion
.
dgn-np:NP193689.RA-CA-GnuDpAOXqhtwHgOtmRqm5NK7QlAUL4mPlQ-PIBc130_provenance
a
np:Provenance
.
dgn-np:NP193689.RA-CA-GnuDpAOXqhtwHgOtmRqm5NK7QlAUL4mPlQ-PIBc130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP193689.RA-CA-GnuDpAOXqhtwHgOtmRqm5NK7QlAUL4mPlQ-PIBc130_assertion
{
miriam-gene:7161
a
ncit:C16612
.
lld:C0014859
a
ncit:C7057
.
dgn-gda:DGNcfb4be6603b30e0ba8f3ea27a3bb74fd
sio:SIO_000628
miriam-gene:7161
,
lld:C0014859
;
a
sio:SIO_001121
.
}
dgn-np:NP193689.RA-CA-GnuDpAOXqhtwHgOtmRqm5NK7QlAUL4mPlQ-PIBc130_provenance
{
dgn-np:NP193689.RA-CA-GnuDpAOXqhtwHgOtmRqm5NK7QlAUL4mPlQ-PIBc130_assertion
dcterms:description
"[Since the 1p36 locus is reported to be deleted and p53 is frequently mutated in esophageal carcinomas, we examined loss of heterozygosity (LOH) and mutation of the p73 gene in 48 untreated esophageal tumors, as well as mRNA expression in 8 tumors.]. 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:9797131
;
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:NP193689.RA-CA-GnuDpAOXqhtwHgOtmRqm5NK7QlAUL4mPlQ-PIBc130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:46+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
<
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
"v2.1.0.0" .
dgn-void:disgenetrdf
pav:version
"v2.1.0" .
}