@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP769848.RA4uYnbjEYZCD14Dpb6kxMljM4k4_nqy5CA2TVkRbHn1c
> .
@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:NP769848.RA4uYnbjEYZCD14Dpb6kxMljM4k4_nqy5CA2TVkRbHn1c130_head
{
this:
np:hasAssertion
dgn-np:NP769848.RA4uYnbjEYZCD14Dpb6kxMljM4k4_nqy5CA2TVkRbHn1c130_assertion
;
np:hasProvenance
dgn-np:NP769848.RA4uYnbjEYZCD14Dpb6kxMljM4k4_nqy5CA2TVkRbHn1c130_provenance
;
np:hasPublicationInfo
dgn-np:NP769848.RA4uYnbjEYZCD14Dpb6kxMljM4k4_nqy5CA2TVkRbHn1c130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP769848.RA4uYnbjEYZCD14Dpb6kxMljM4k4_nqy5CA2TVkRbHn1c130_assertion
a
np:Assertion
.
dgn-np:NP769848.RA4uYnbjEYZCD14Dpb6kxMljM4k4_nqy5CA2TVkRbHn1c130_provenance
a
np:Provenance
.
dgn-np:NP769848.RA4uYnbjEYZCD14Dpb6kxMljM4k4_nqy5CA2TVkRbHn1c130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP769848.RA4uYnbjEYZCD14Dpb6kxMljM4k4_nqy5CA2TVkRbHn1c130_assertion
{
miriam-gene:1029
a
ncit:C16612
.
lld:C0751688
a
ncit:C7057
.
dgn-gda:DGN86c22609e0334332c9306e2367c1124c
sio:SIO_000628
miriam-gene:1029
,
lld:C0751688
;
a
sio:SIO_001121
.
}
dgn-np:NP769848.RA4uYnbjEYZCD14Dpb6kxMljM4k4_nqy5CA2TVkRbHn1c130_provenance
{
dgn-np:NP769848.RA4uYnbjEYZCD14Dpb6kxMljM4k4_nqy5CA2TVkRbHn1c130_assertion
dcterms:description
"[The aim of our study was to analyze the relationship between genetic changes leading to inactivation of the CDKN2A gene and subsequent alteration of protein expression in squamous cell cancer of the larynx (SCCL) in connection with the clinical and histopathological course of the disease.]. 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:14991744
;
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:NP769848.RA4uYnbjEYZCD14Dpb6kxMljM4k4_nqy5CA2TVkRbHn1c130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:45+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" .
}