@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP512252.RAA068N-nDE259BeHCw6c01zeajIAF8GjciObR1R_usko
> .
@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:NP512252.RAA068N-nDE259BeHCw6c01zeajIAF8GjciObR1R_usko130_head
{
this:
np:hasAssertion
dgn-np:NP512252.RAA068N-nDE259BeHCw6c01zeajIAF8GjciObR1R_usko130_assertion
;
np:hasProvenance
dgn-np:NP512252.RAA068N-nDE259BeHCw6c01zeajIAF8GjciObR1R_usko130_provenance
;
np:hasPublicationInfo
dgn-np:NP512252.RAA068N-nDE259BeHCw6c01zeajIAF8GjciObR1R_usko130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP512252.RAA068N-nDE259BeHCw6c01zeajIAF8GjciObR1R_usko130_assertion
a
np:Assertion
.
dgn-np:NP512252.RAA068N-nDE259BeHCw6c01zeajIAF8GjciObR1R_usko130_provenance
a
np:Provenance
.
dgn-np:NP512252.RAA068N-nDE259BeHCw6c01zeajIAF8GjciObR1R_usko130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP512252.RAA068N-nDE259BeHCw6c01zeajIAF8GjciObR1R_usko130_assertion
{
miriam-gene:50514
a
ncit:C16612
.
lld:C0152018
a
ncit:C7057
.
dgn-gda:DGN900071d993916c823ae19fe1f1a47721
sio:SIO_000628
miriam-gene:50514
,
lld:C0152018
;
a
sio:SIO_001121
.
}
dgn-np:NP512252.RAA068N-nDE259BeHCw6c01zeajIAF8GjciObR1R_usko130_provenance
{
dgn-np:NP512252.RAA068N-nDE259BeHCw6c01zeajIAF8GjciObR1R_usko130_assertion
dcterms:description
"[Given the reduced expression of the DEC1 gene in esophageal cancer, the high frequency of LOH at 9q32 in esophageal carcinomas, and the fact that the DEC1 cDNA can suppress growth of some cancer cells in vitro, we suggest that the DEC1 gene is a candidate tumor suppressor in 9q32.]. 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:10612805
;
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:NP512252.RAA068N-nDE259BeHCw6c01zeajIAF8GjciObR1R_usko130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:05+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" .
}