@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP158881.RAbqPEX4SlcCbyCv1iO9Ctjm2R8_zK5qYq5PPGBgRjPH8
> .
@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:NP158881.RAbqPEX4SlcCbyCv1iO9Ctjm2R8_zK5qYq5PPGBgRjPH8130_head
{
this:
np:hasAssertion
dgn-np:NP158881.RAbqPEX4SlcCbyCv1iO9Ctjm2R8_zK5qYq5PPGBgRjPH8130_assertion
;
np:hasProvenance
dgn-np:NP158881.RAbqPEX4SlcCbyCv1iO9Ctjm2R8_zK5qYq5PPGBgRjPH8130_provenance
;
np:hasPublicationInfo
dgn-np:NP158881.RAbqPEX4SlcCbyCv1iO9Ctjm2R8_zK5qYq5PPGBgRjPH8130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP158881.RAbqPEX4SlcCbyCv1iO9Ctjm2R8_zK5qYq5PPGBgRjPH8130_assertion
a
np:Assertion
.
dgn-np:NP158881.RAbqPEX4SlcCbyCv1iO9Ctjm2R8_zK5qYq5PPGBgRjPH8130_provenance
a
np:Provenance
.
dgn-np:NP158881.RAbqPEX4SlcCbyCv1iO9Ctjm2R8_zK5qYq5PPGBgRjPH8130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP158881.RAbqPEX4SlcCbyCv1iO9Ctjm2R8_zK5qYq5PPGBgRjPH8130_assertion
{
miriam-gene:7157
a
ncit:C16612
.
lld:C0002448
a
ncit:C7057
.
dgn-gda:DGNeb95667a8d27367f4533bd14ef5854d6
sio:SIO_000628
miriam-gene:7157
,
lld:C0002448
;
a
sio:SIO_001121
.
}
dgn-np:NP158881.RAbqPEX4SlcCbyCv1iO9Ctjm2R8_zK5qYq5PPGBgRjPH8130_provenance
{
dgn-np:NP158881.RAbqPEX4SlcCbyCv1iO9Ctjm2R8_zK5qYq5PPGBgRjPH8130_assertion
dcterms:description
"[We concluded that PCNA overexpression is not responsible for the difference in clinical behavior of these two lesions, whereas the expression of p53 in ameloblastoma may explain the more aggressive nature of this tumor compared with AOT.]. 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:21712626
;
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:NP158881.RAbqPEX4SlcCbyCv1iO9Ctjm2R8_zK5qYq5PPGBgRjPH8130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:25+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" .
}