@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP276364.RAmi-hpeDwnXdxE1-p-7J46aAEUG-puv2rtpFVoHBVLxs
> .
@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:NP276364.RAmi-hpeDwnXdxE1-p-7J46aAEUG-puv2rtpFVoHBVLxs130_head
{
this:
np:hasAssertion
dgn-np:NP276364.RAmi-hpeDwnXdxE1-p-7J46aAEUG-puv2rtpFVoHBVLxs130_assertion
;
np:hasProvenance
dgn-np:NP276364.RAmi-hpeDwnXdxE1-p-7J46aAEUG-puv2rtpFVoHBVLxs130_provenance
;
np:hasPublicationInfo
dgn-np:NP276364.RAmi-hpeDwnXdxE1-p-7J46aAEUG-puv2rtpFVoHBVLxs130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP276364.RAmi-hpeDwnXdxE1-p-7J46aAEUG-puv2rtpFVoHBVLxs130_assertion
a
np:Assertion
.
dgn-np:NP276364.RAmi-hpeDwnXdxE1-p-7J46aAEUG-puv2rtpFVoHBVLxs130_provenance
a
np:Provenance
.
dgn-np:NP276364.RAmi-hpeDwnXdxE1-p-7J46aAEUG-puv2rtpFVoHBVLxs130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP276364.RAmi-hpeDwnXdxE1-p-7J46aAEUG-puv2rtpFVoHBVLxs130_assertion
{
miriam-gene:595
a
ncit:C16612
.
lld:C0175754
a
ncit:C7057
.
dgn-gda:DGN54a114a08d0be70d06d74b138805ed28
sio:SIO_000628
miriam-gene:595
,
lld:C0175754
;
a
sio:SIO_001121
.
}
dgn-np:NP276364.RAmi-hpeDwnXdxE1-p-7J46aAEUG-puv2rtpFVoHBVLxs130_provenance
{
dgn-np:NP276364.RAmi-hpeDwnXdxE1-p-7J46aAEUG-puv2rtpFVoHBVLxs130_assertion
dcterms:description
"[These findings suggested, however, alternations of Rb pathway were infrequent events in ACC of salivary glands and inactivation of p16INK4A, cyclin D1 overexpression may be related to the high cell proliferating activity of ACC.]. 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:10928172
;
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:NP276364.RAmi-hpeDwnXdxE1-p-7J46aAEUG-puv2rtpFVoHBVLxs130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:35+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" .
}