@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP365223.RAyPL3HmZwoBW6tk0m21YA0R0ztgA-_ZwgtWBDR-Tmy-s
> .
@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:NP365223.RAyPL3HmZwoBW6tk0m21YA0R0ztgA-_ZwgtWBDR-Tmy-s130_head
{
this:
np:hasAssertion
dgn-np:NP365223.RAyPL3HmZwoBW6tk0m21YA0R0ztgA-_ZwgtWBDR-Tmy-s130_assertion
;
np:hasProvenance
dgn-np:NP365223.RAyPL3HmZwoBW6tk0m21YA0R0ztgA-_ZwgtWBDR-Tmy-s130_provenance
;
np:hasPublicationInfo
dgn-np:NP365223.RAyPL3HmZwoBW6tk0m21YA0R0ztgA-_ZwgtWBDR-Tmy-s130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP365223.RAyPL3HmZwoBW6tk0m21YA0R0ztgA-_ZwgtWBDR-Tmy-s130_assertion
a
np:Assertion
.
dgn-np:NP365223.RAyPL3HmZwoBW6tk0m21YA0R0ztgA-_ZwgtWBDR-Tmy-s130_provenance
a
np:Provenance
.
dgn-np:NP365223.RAyPL3HmZwoBW6tk0m21YA0R0ztgA-_ZwgtWBDR-Tmy-s130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP365223.RAyPL3HmZwoBW6tk0m21YA0R0ztgA-_ZwgtWBDR-Tmy-s130_assertion
{
miriam-gene:1029
a
ncit:C16612
.
lld:C0007099
a
ncit:C7057
.
dgn-gda:DGN64aa653b2b16a5a375b270e3c4b36149
sio:SIO_000628
miriam-gene:1029
,
lld:C0007099
;
a
sio:SIO_001121
.
}
dgn-np:NP365223.RAyPL3HmZwoBW6tk0m21YA0R0ztgA-_ZwgtWBDR-Tmy-s130_provenance
{
dgn-np:NP365223.RAyPL3HmZwoBW6tk0m21YA0R0ztgA-_ZwgtWBDR-Tmy-s130_assertion
dcterms:description
"[p16 was not detectable in benign hyperplastic lesions, but instead was expressed heterogeneously in some dysplastic and carcinoma in situ lesions and consistently at areas of microinvasion and at superficial margins of advanced SCCs.]. 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:12875969
;
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:NP365223.RAyPL3HmZwoBW6tk0m21YA0R0ztgA-_ZwgtWBDR-Tmy-s130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:34+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" .
}