@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP1330258.RAQ7_G-MHKWif7ejHfulIpwCDjXuhm9JmdUvcLYUweljg
> .
@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/
> .
dgn-np:NP1330258.RAQ7_G-MHKWif7ejHfulIpwCDjXuhm9JmdUvcLYUweljg130_head
{
this:
np:hasAssertion
dgn-np:NP1330258.RAQ7_G-MHKWif7ejHfulIpwCDjXuhm9JmdUvcLYUweljg130_assertion
;
np:hasProvenance
dgn-np:NP1330258.RAQ7_G-MHKWif7ejHfulIpwCDjXuhm9JmdUvcLYUweljg130_provenance
;
np:hasPublicationInfo
dgn-np:NP1330258.RAQ7_G-MHKWif7ejHfulIpwCDjXuhm9JmdUvcLYUweljg130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP1330258.RAQ7_G-MHKWif7ejHfulIpwCDjXuhm9JmdUvcLYUweljg130_assertion
a
np:Assertion
.
dgn-np:NP1330258.RAQ7_G-MHKWif7ejHfulIpwCDjXuhm9JmdUvcLYUweljg130_provenance
a
np:Provenance
.
dgn-np:NP1330258.RAQ7_G-MHKWif7ejHfulIpwCDjXuhm9JmdUvcLYUweljg130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP1330258.RAQ7_G-MHKWif7ejHfulIpwCDjXuhm9JmdUvcLYUweljg130_assertion
{
miriam-gene:7157
a
ncit:C16612
.
lld:C0014859
a
ncit:C7057
.
dgn-gda:DGN52333764548181922770fc9fadcaa6c8
sio:SIO_000628
miriam-gene:7157
,
lld:C0014859
;
a
sio:SIO_001121
.
}
dgn-np:NP1330258.RAQ7_G-MHKWif7ejHfulIpwCDjXuhm9JmdUvcLYUweljg130_provenance
{
dgn-np:NP1330258.RAQ7_G-MHKWif7ejHfulIpwCDjXuhm9JmdUvcLYUweljg130_assertion
dcterms:description
"[Our study shows that p53 point mutations occur more frequently in patients with esophageal cancer from this region than in patients from other areas of the world where the disease is prevalent.]. 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:8028358
;
prov:wasDerivedFrom
dgn-void:befree-2016
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-2016
pav:importedOn
"2016-02-19"^^
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:NP1330258.RAQ7_G-MHKWif7ejHfulIpwCDjXuhm9JmdUvcLYUweljg130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:51:49+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:disgenetv3.0rdf
;
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
"v4.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v4.0.0" .
}