@prefix dc: <
http://purl.org/dc/terms/
> .
@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP80282.RAZJaEndlAnBu334yXrU0O4jj2A051r0uGkCkG6wLguuc
> .
@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 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:NP80282.RAZJaEndlAnBu334yXrU0O4jj2A051r0uGkCkG6wLguuc130_head
{
this:
np:hasAssertion
dgn-np:NP80282.RAZJaEndlAnBu334yXrU0O4jj2A051r0uGkCkG6wLguuc130_assertion
;
np:hasProvenance
dgn-np:NP80282.RAZJaEndlAnBu334yXrU0O4jj2A051r0uGkCkG6wLguuc130_provenance
;
np:hasPublicationInfo
dgn-np:NP80282.RAZJaEndlAnBu334yXrU0O4jj2A051r0uGkCkG6wLguuc130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP80282.RAZJaEndlAnBu334yXrU0O4jj2A051r0uGkCkG6wLguuc130_assertion
a
np:Assertion
.
dgn-np:NP80282.RAZJaEndlAnBu334yXrU0O4jj2A051r0uGkCkG6wLguuc130_provenance
a
np:Provenance
.
dgn-np:NP80282.RAZJaEndlAnBu334yXrU0O4jj2A051r0uGkCkG6wLguuc130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP80282.RAZJaEndlAnBu334yXrU0O4jj2A051r0uGkCkG6wLguuc130_assertion
{
miriam-gene:7157
a
ncit:C16612
.
lld:C0038356
a
ncit:C7057
.
dgn-gda:DGNdcfe3f222e9fed5aabf34b13032d3e9a
sio:SIO_000628
miriam-gene:7157
,
lld:C0038356
;
a
sio:SIO_001122
.
}
dgn-np:NP80282.RAZJaEndlAnBu334yXrU0O4jj2A051r0uGkCkG6wLguuc130_provenance
{
dgn-np:NP80282.RAZJaEndlAnBu334yXrU0O4jj2A051r0uGkCkG6wLguuc130_assertion
dc:description
"[this study suggests that the p53 codon 72 polymorphism may be associated with gastric cancer in Chinese Han patients, and that difference in genotype distribution may be associated with the location and stage of gastric cancer.]. 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:20939739
;
prov:wasDerivedFrom
dgn-void:gad-20130706
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:gad-20130706
pav:importedOn
"2013-07-06"^^
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:NP80282.RAZJaEndlAnBu334yXrU0O4jj2A051r0uGkCkG6wLguuc130_publicationInfo
{
this:
dc:created
"2014-10-02T12:32:39+02:00"^^
xsd:dateTime
;
dc:rights
<
http://opendatacommons.org/licenses/odbl/1.0/
> ;
dc:rightsHolder
dgn-void:IBIGroup
;
dc: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" .
}