@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP794282.RA-DmIFjdQKBRca0m7Fw2bRffmIKEoUS78IHqpzM8gK94
> .
@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:NP794282.RA-DmIFjdQKBRca0m7Fw2bRffmIKEoUS78IHqpzM8gK94130_head
{
this:
np:hasAssertion
dgn-np:NP794282.RA-DmIFjdQKBRca0m7Fw2bRffmIKEoUS78IHqpzM8gK94130_assertion
;
np:hasProvenance
dgn-np:NP794282.RA-DmIFjdQKBRca0m7Fw2bRffmIKEoUS78IHqpzM8gK94130_provenance
;
np:hasPublicationInfo
dgn-np:NP794282.RA-DmIFjdQKBRca0m7Fw2bRffmIKEoUS78IHqpzM8gK94130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP794282.RA-DmIFjdQKBRca0m7Fw2bRffmIKEoUS78IHqpzM8gK94130_assertion
a
np:Assertion
.
dgn-np:NP794282.RA-DmIFjdQKBRca0m7Fw2bRffmIKEoUS78IHqpzM8gK94130_provenance
a
np:Provenance
.
dgn-np:NP794282.RA-DmIFjdQKBRca0m7Fw2bRffmIKEoUS78IHqpzM8gK94130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP794282.RA-DmIFjdQKBRca0m7Fw2bRffmIKEoUS78IHqpzM8gK94130_assertion
{
miriam-gene:7157
a
ncit:C16612
.
lld:C0870082
a
ncit:C7057
.
dgn-gda:DGN6493610a53671e724435433af3c55424
sio:SIO_000628
miriam-gene:7157
,
lld:C0870082
;
a
sio:SIO_001121
.
}
dgn-np:NP794282.RA-DmIFjdQKBRca0m7Fw2bRffmIKEoUS78IHqpzM8gK94130_provenance
{
dgn-np:NP794282.RA-DmIFjdQKBRca0m7Fw2bRffmIKEoUS78IHqpzM8gK94130_assertion
dcterms:description
"[Samples from 54 patients with OSCC, 45 with oral lichen planus (OLP) and 45 with hyperkeratosis (clinically leukoplakia), diagnosed between 1987 and 1996, were analysed for TP53 protein expression and TP53 mutation.]. 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:19473450
;
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:NP794282.RA-DmIFjdQKBRca0m7Fw2bRffmIKEoUS78IHqpzM8gK94130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:08+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" .
}