@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP758256.RAFAJg1e8Kyrc9HDOvFGVznOSi8hW-0777LIgcS3AnHwc
> .
@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:NP758256.RAFAJg1e8Kyrc9HDOvFGVznOSi8hW-0777LIgcS3AnHwc130_head
{
this:
np:hasAssertion
dgn-np:NP758256.RAFAJg1e8Kyrc9HDOvFGVznOSi8hW-0777LIgcS3AnHwc130_assertion
;
np:hasProvenance
dgn-np:NP758256.RAFAJg1e8Kyrc9HDOvFGVznOSi8hW-0777LIgcS3AnHwc130_provenance
;
np:hasPublicationInfo
dgn-np:NP758256.RAFAJg1e8Kyrc9HDOvFGVznOSi8hW-0777LIgcS3AnHwc130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP758256.RAFAJg1e8Kyrc9HDOvFGVznOSi8hW-0777LIgcS3AnHwc130_assertion
a
np:Assertion
.
dgn-np:NP758256.RAFAJg1e8Kyrc9HDOvFGVznOSi8hW-0777LIgcS3AnHwc130_provenance
a
np:Provenance
.
dgn-np:NP758256.RAFAJg1e8Kyrc9HDOvFGVznOSi8hW-0777LIgcS3AnHwc130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP758256.RAFAJg1e8Kyrc9HDOvFGVznOSi8hW-0777LIgcS3AnHwc130_assertion
{
miriam-gene:23549
a
ncit:C16612
.
lld:C1168401
a
ncit:C7057
.
dgn-gda:DGNea6712bdd2c9f5fbba1231c4fb3fb2b1
sio:SIO_000628
miriam-gene:23549
,
lld:C1168401
;
a
sio:SIO_001121
.
}
dgn-np:NP758256.RAFAJg1e8Kyrc9HDOvFGVznOSi8hW-0777LIgcS3AnHwc130_provenance
{
dgn-np:NP758256.RAFAJg1e8Kyrc9HDOvFGVznOSi8hW-0777LIgcS3AnHwc130_assertion
dcterms:description
"[In order to study the association of tumor suppressor gene promoter methylation in HNSCC with patient clinical characteristics, especially alcohol consumption and tobacco smoking, we examined promoter methylation of the p16(INK4a), DAP-kinase, E-Cadherin, and RASSF1A genes using methylation-specific PCR (MSP) in 80 patients.]. 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:12082610
;
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:NP758256.RAFAJg1e8Kyrc9HDOvFGVznOSi8hW-0777LIgcS3AnHwc130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:39+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" .
}