@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP815953.RAyq0s3O33BQzV0y_S5QpQRV7L0LEudxlwAkT6MAFjg3c
> .
@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:NP815953.RAyq0s3O33BQzV0y_S5QpQRV7L0LEudxlwAkT6MAFjg3c130_head
{
this:
np:hasAssertion
dgn-np:NP815953.RAyq0s3O33BQzV0y_S5QpQRV7L0LEudxlwAkT6MAFjg3c130_assertion
;
np:hasProvenance
dgn-np:NP815953.RAyq0s3O33BQzV0y_S5QpQRV7L0LEudxlwAkT6MAFjg3c130_provenance
;
np:hasPublicationInfo
dgn-np:NP815953.RAyq0s3O33BQzV0y_S5QpQRV7L0LEudxlwAkT6MAFjg3c130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP815953.RAyq0s3O33BQzV0y_S5QpQRV7L0LEudxlwAkT6MAFjg3c130_assertion
a
np:Assertion
.
dgn-np:NP815953.RAyq0s3O33BQzV0y_S5QpQRV7L0LEudxlwAkT6MAFjg3c130_provenance
a
np:Provenance
.
dgn-np:NP815953.RAyq0s3O33BQzV0y_S5QpQRV7L0LEudxlwAkT6MAFjg3c130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP815953.RAyq0s3O33BQzV0y_S5QpQRV7L0LEudxlwAkT6MAFjg3c130_assertion
{
miriam-gene:7157
a
ncit:C16612
.
lld:C0014818
a
ncit:C7057
.
dgn-gda:DGNcd1228700d87c83a69bc65867d48798f
sio:SIO_000628
miriam-gene:7157
,
lld:C0014818
;
a
sio:SIO_001121
.
}
dgn-np:NP815953.RAyq0s3O33BQzV0y_S5QpQRV7L0LEudxlwAkT6MAFjg3c130_provenance
{
dgn-np:NP815953.RAyq0s3O33BQzV0y_S5QpQRV7L0LEudxlwAkT6MAFjg3c130_assertion
dcterms:description
"[The availability of strains of partially transformed keratinocytes from premalignant erythroplakias which possess normal p53 genes should enable us to test the role of mutant p53 in the progression of erythroplakia to SCC.]. 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:7917902
;
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:NP815953.RAyq0s3O33BQzV0y_S5QpQRV7L0LEudxlwAkT6MAFjg3c130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:20+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" .
}