@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP490951.RAvXbI40Gt0T1G1JJTGbCKU6ImWGESUVws1ZoFPj6CjuU
> .
@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:NP490951.RAvXbI40Gt0T1G1JJTGbCKU6ImWGESUVws1ZoFPj6CjuU130_head
{
this:
np:hasAssertion
dgn-np:NP490951.RAvXbI40Gt0T1G1JJTGbCKU6ImWGESUVws1ZoFPj6CjuU130_assertion
;
np:hasProvenance
dgn-np:NP490951.RAvXbI40Gt0T1G1JJTGbCKU6ImWGESUVws1ZoFPj6CjuU130_provenance
;
np:hasPublicationInfo
dgn-np:NP490951.RAvXbI40Gt0T1G1JJTGbCKU6ImWGESUVws1ZoFPj6CjuU130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP490951.RAvXbI40Gt0T1G1JJTGbCKU6ImWGESUVws1ZoFPj6CjuU130_assertion
a
np:Assertion
.
dgn-np:NP490951.RAvXbI40Gt0T1G1JJTGbCKU6ImWGESUVws1ZoFPj6CjuU130_provenance
a
np:Provenance
.
dgn-np:NP490951.RAvXbI40Gt0T1G1JJTGbCKU6ImWGESUVws1ZoFPj6CjuU130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP490951.RAvXbI40Gt0T1G1JJTGbCKU6ImWGESUVws1ZoFPj6CjuU130_assertion
{
miriam-gene:3081
a
ncit:C16612
.
lld:C0007097
a
ncit:C7057
.
dgn-gda:DGNbc69ed9762327923e5cc992b465e1904
sio:SIO_000628
miriam-gene:3081
,
lld:C0007097
;
a
sio:SIO_001121
.
}
dgn-np:NP490951.RAvXbI40Gt0T1G1JJTGbCKU6ImWGESUVws1ZoFPj6CjuU130_provenance
{
dgn-np:NP490951.RAvXbI40Gt0T1G1JJTGbCKU6ImWGESUVws1ZoFPj6CjuU130_assertion
dcterms:description
"[One possible conclusion from this comparison is that the higher proportion of flat neoplastic colorectal lesions with HGD and carcinoma in the Japanese (compared with the Swedish) takes place for reasons extraneous to the overexpression of the p53 protein.]. 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:8620779
;
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:NP490951.RAvXbI40Gt0T1G1JJTGbCKU6ImWGESUVws1ZoFPj6CjuU130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:53+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" .
}