@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP822604.RApIXkE2d0m_yqIXRiEdJnuTfTQLkBwdDKVWc64_mT9qw
> .
@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:NP822604.RApIXkE2d0m_yqIXRiEdJnuTfTQLkBwdDKVWc64_mT9qw130_head
{
this:
np:hasAssertion
dgn-np:NP822604.RApIXkE2d0m_yqIXRiEdJnuTfTQLkBwdDKVWc64_mT9qw130_assertion
;
np:hasProvenance
dgn-np:NP822604.RApIXkE2d0m_yqIXRiEdJnuTfTQLkBwdDKVWc64_mT9qw130_provenance
;
np:hasPublicationInfo
dgn-np:NP822604.RApIXkE2d0m_yqIXRiEdJnuTfTQLkBwdDKVWc64_mT9qw130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP822604.RApIXkE2d0m_yqIXRiEdJnuTfTQLkBwdDKVWc64_mT9qw130_assertion
a
np:Assertion
.
dgn-np:NP822604.RApIXkE2d0m_yqIXRiEdJnuTfTQLkBwdDKVWc64_mT9qw130_provenance
a
np:Provenance
.
dgn-np:NP822604.RApIXkE2d0m_yqIXRiEdJnuTfTQLkBwdDKVWc64_mT9qw130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP822604.RApIXkE2d0m_yqIXRiEdJnuTfTQLkBwdDKVWc64_mT9qw130_assertion
{
miriam-gene:7157
a
ncit:C16612
.
lld:C0026640
a
ncit:C7057
.
dgn-gda:DGN61719d90cbbe58f9520874aea754b1f5
sio:SIO_000628
miriam-gene:7157
,
lld:C0026640
;
a
sio:SIO_001121
.
}
dgn-np:NP822604.RApIXkE2d0m_yqIXRiEdJnuTfTQLkBwdDKVWc64_mT9qw130_provenance
{
dgn-np:NP822604.RApIXkE2d0m_yqIXRiEdJnuTfTQLkBwdDKVWc64_mT9qw130_assertion
dcterms:description
"[The present data indicate that p53 mutations are extremely frequent in oral cancers in the Japanese, and suggest that the timing and significance of p53 mutation in oral tumor progression vary in different ethnic populations and areas.]. 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:9400993
;
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:NP822604.RApIXkE2d0m_yqIXRiEdJnuTfTQLkBwdDKVWc64_mT9qw130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:24+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" .
}