@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP215176.RAqyP8n-CCBsix6nlz2JyTXmsgZe7fdGtpM5Uz4UfseDg
> .
@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:NP215176.RAqyP8n-CCBsix6nlz2JyTXmsgZe7fdGtpM5Uz4UfseDg130_head
{
this:
np:hasAssertion
dgn-np:NP215176.RAqyP8n-CCBsix6nlz2JyTXmsgZe7fdGtpM5Uz4UfseDg130_assertion
;
np:hasProvenance
dgn-np:NP215176.RAqyP8n-CCBsix6nlz2JyTXmsgZe7fdGtpM5Uz4UfseDg130_provenance
;
np:hasPublicationInfo
dgn-np:NP215176.RAqyP8n-CCBsix6nlz2JyTXmsgZe7fdGtpM5Uz4UfseDg130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP215176.RAqyP8n-CCBsix6nlz2JyTXmsgZe7fdGtpM5Uz4UfseDg130_assertion
a
np:Assertion
.
dgn-np:NP215176.RAqyP8n-CCBsix6nlz2JyTXmsgZe7fdGtpM5Uz4UfseDg130_provenance
a
np:Provenance
.
dgn-np:NP215176.RAqyP8n-CCBsix6nlz2JyTXmsgZe7fdGtpM5Uz4UfseDg130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP215176.RAqyP8n-CCBsix6nlz2JyTXmsgZe7fdGtpM5Uz4UfseDg130_assertion
{
miriam-gene:1030
a
ncit:C16612
.
lld:C0007137
a
ncit:C7057
.
dgn-gda:DGN79ed91e4ca65dce56146fe7fbbdf4933
sio:SIO_000628
miriam-gene:1030
,
lld:C0007137
;
a
sio:SIO_001121
.
}
dgn-np:NP215176.RAqyP8n-CCBsix6nlz2JyTXmsgZe7fdGtpM5Uz4UfseDg130_provenance
{
dgn-np:NP215176.RAqyP8n-CCBsix6nlz2JyTXmsgZe7fdGtpM5Uz4UfseDg130_assertion
dcterms:description
"[Thus, our data suggest that, except for p15/16 and MTAP gene, there were at least two candidate tumor suppressor genes located at chromosome 9p, and that the alteration of these genes is associated with the tumorigenesis of oral SCC.]. 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:10226521
;
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:NP215176.RAqyP8n-CCBsix6nlz2JyTXmsgZe7fdGtpM5Uz4UfseDg130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:59+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" .
}