@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP118488.RAdvXdq-dBnTbUxWXvSKLU8acaq96AevFFmglgRUZfgFM
> .
@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:NP118488.RAdvXdq-dBnTbUxWXvSKLU8acaq96AevFFmglgRUZfgFM130_head
{
this:
np:hasAssertion
dgn-np:NP118488.RAdvXdq-dBnTbUxWXvSKLU8acaq96AevFFmglgRUZfgFM130_assertion
;
np:hasProvenance
dgn-np:NP118488.RAdvXdq-dBnTbUxWXvSKLU8acaq96AevFFmglgRUZfgFM130_provenance
;
np:hasPublicationInfo
dgn-np:NP118488.RAdvXdq-dBnTbUxWXvSKLU8acaq96AevFFmglgRUZfgFM130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP118488.RAdvXdq-dBnTbUxWXvSKLU8acaq96AevFFmglgRUZfgFM130_assertion
a
np:Assertion
.
dgn-np:NP118488.RAdvXdq-dBnTbUxWXvSKLU8acaq96AevFFmglgRUZfgFM130_provenance
a
np:Provenance
.
dgn-np:NP118488.RAdvXdq-dBnTbUxWXvSKLU8acaq96AevFFmglgRUZfgFM130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP118488.RAdvXdq-dBnTbUxWXvSKLU8acaq96AevFFmglgRUZfgFM130_assertion
{
miriam-gene:7157
a
ncit:C16612
.
lld:C0025202
a
ncit:C7057
.
dgn-gda:DGN565ef42fb393b1372e28154222d267fb
sio:SIO_000628
miriam-gene:7157
,
lld:C0025202
;
a
sio:SIO_001123
.
}
dgn-np:NP118488.RAdvXdq-dBnTbUxWXvSKLU8acaq96AevFFmglgRUZfgFM130_provenance
{
dgn-np:NP118488.RAdvXdq-dBnTbUxWXvSKLU8acaq96AevFFmglgRUZfgFM130_assertion
dcterms:description
"[p53 alterations commence as early as at the stage of benign and dysplastic nevi but there is no concordance between the frequent p53 protein expression and the rarity of both TP53 gene mutations in melanomas.]. 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:15557758
;
prov:wasDerivedFrom
dgn-void:lhgdn-20090331
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:lhgdn-20090331
pav:importedOn
"2009-03-31"^^
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:NP118488.RAdvXdq-dBnTbUxWXvSKLU8acaq96AevFFmglgRUZfgFM130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:01+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" .
}