@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP118415.RAuUN9JwN7UkLBy7uqZ0-ny717Iuxe7LaHIjvv47Cma1k
> .
@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:NP118415.RAuUN9JwN7UkLBy7uqZ0-ny717Iuxe7LaHIjvv47Cma1k130_head
{
this:
np:hasAssertion
dgn-np:NP118415.RAuUN9JwN7UkLBy7uqZ0-ny717Iuxe7LaHIjvv47Cma1k130_assertion
;
np:hasProvenance
dgn-np:NP118415.RAuUN9JwN7UkLBy7uqZ0-ny717Iuxe7LaHIjvv47Cma1k130_provenance
;
np:hasPublicationInfo
dgn-np:NP118415.RAuUN9JwN7UkLBy7uqZ0-ny717Iuxe7LaHIjvv47Cma1k130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP118415.RAuUN9JwN7UkLBy7uqZ0-ny717Iuxe7LaHIjvv47Cma1k130_assertion
a
np:Assertion
.
dgn-np:NP118415.RAuUN9JwN7UkLBy7uqZ0-ny717Iuxe7LaHIjvv47Cma1k130_provenance
a
np:Provenance
.
dgn-np:NP118415.RAuUN9JwN7UkLBy7uqZ0-ny717Iuxe7LaHIjvv47Cma1k130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP118415.RAuUN9JwN7UkLBy7uqZ0-ny717Iuxe7LaHIjvv47Cma1k130_assertion
{
miriam-gene:1029
a
ncit:C16612
.
lld:C0025202
a
ncit:C7057
.
dgn-gda:DGN96ab95f707a9696fa5c3ef93b170a5fe
sio:SIO_000628
miriam-gene:1029
,
lld:C0025202
;
a
sio:SIO_001124
.
}
dgn-np:NP118415.RAuUN9JwN7UkLBy7uqZ0-ny717Iuxe7LaHIjvv47Cma1k130_provenance
{
dgn-np:NP118415.RAuUN9JwN7UkLBy7uqZ0-ny717Iuxe7LaHIjvv47Cma1k130_assertion
dcterms:description
"[Genetic and epigenetic analyses of the human 9p21 locus indicate that modifications of ARF occur independently of p16 inactivation in human melanoma and suggest that ARF is more frequently inactivated than p16.]. 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:18505964
;
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:NP118415.RAuUN9JwN7UkLBy7uqZ0-ny717Iuxe7LaHIjvv47Cma1k130_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" .
}