@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP486291.RAl47g5JyALReu-lRATNwDCWBnqgAvEgaYy9W4RsTPlEo
> .
@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:NP486291.RAl47g5JyALReu-lRATNwDCWBnqgAvEgaYy9W4RsTPlEo130_head
{
this:
np:hasAssertion
dgn-np:NP486291.RAl47g5JyALReu-lRATNwDCWBnqgAvEgaYy9W4RsTPlEo130_assertion
;
np:hasProvenance
dgn-np:NP486291.RAl47g5JyALReu-lRATNwDCWBnqgAvEgaYy9W4RsTPlEo130_provenance
;
np:hasPublicationInfo
dgn-np:NP486291.RAl47g5JyALReu-lRATNwDCWBnqgAvEgaYy9W4RsTPlEo130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP486291.RAl47g5JyALReu-lRATNwDCWBnqgAvEgaYy9W4RsTPlEo130_assertion
a
np:Assertion
.
dgn-np:NP486291.RAl47g5JyALReu-lRATNwDCWBnqgAvEgaYy9W4RsTPlEo130_provenance
a
np:Provenance
.
dgn-np:NP486291.RAl47g5JyALReu-lRATNwDCWBnqgAvEgaYy9W4RsTPlEo130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP486291.RAl47g5JyALReu-lRATNwDCWBnqgAvEgaYy9W4RsTPlEo130_assertion
{
miriam-gene:1029
a
ncit:C16612
.
lld:C1332922
a
ncit:C7057
.
dgn-gda:DGNeab8b3acda9d4a1f31aa3265a4690abe
sio:SIO_000628
miriam-gene:1029
,
lld:C1332922
;
a
sio:SIO_001121
.
}
dgn-np:NP486291.RAl47g5JyALReu-lRATNwDCWBnqgAvEgaYy9W4RsTPlEo130_provenance
{
dgn-np:NP486291.RAl47g5JyALReu-lRATNwDCWBnqgAvEgaYy9W4RsTPlEo130_assertion
dcterms:description
"[The quantitative evaluation of p16 INK4A expression by CL IHC assay could be therefore an interesting adjuvant method to distinguish different CIN grades and to predict the risk of progression of early CIN lesions.]. 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:18753961
;
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:NP486291.RAl47g5JyALReu-lRATNwDCWBnqgAvEgaYy9W4RsTPlEo130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:50+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" .
}