@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP144569.RAZDX59RV99nvHsz9J3rfwezbmJvlV4_sxvK6x3hU-Rp4
> .
@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:NP144569.RAZDX59RV99nvHsz9J3rfwezbmJvlV4_sxvK6x3hU-Rp4130_head
{
this:
np:hasAssertion
dgn-np:NP144569.RAZDX59RV99nvHsz9J3rfwezbmJvlV4_sxvK6x3hU-Rp4130_assertion
;
np:hasProvenance
dgn-np:NP144569.RAZDX59RV99nvHsz9J3rfwezbmJvlV4_sxvK6x3hU-Rp4130_provenance
;
np:hasPublicationInfo
dgn-np:NP144569.RAZDX59RV99nvHsz9J3rfwezbmJvlV4_sxvK6x3hU-Rp4130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP144569.RAZDX59RV99nvHsz9J3rfwezbmJvlV4_sxvK6x3hU-Rp4130_assertion
a
np:Assertion
.
dgn-np:NP144569.RAZDX59RV99nvHsz9J3rfwezbmJvlV4_sxvK6x3hU-Rp4130_provenance
a
np:Provenance
.
dgn-np:NP144569.RAZDX59RV99nvHsz9J3rfwezbmJvlV4_sxvK6x3hU-Rp4130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP144569.RAZDX59RV99nvHsz9J3rfwezbmJvlV4_sxvK6x3hU-Rp4130_assertion
{
miriam-gene:4255
a
ncit:C16612
.
lld:C0032580
a
ncit:C7057
.
dgn-gda:DGNba5d4d6f50a01b246707374c489c7005
sio:SIO_000628
miriam-gene:4255
,
lld:C0032580
;
a
sio:SIO_001123
.
}
dgn-np:NP144569.RAZDX59RV99nvHsz9J3rfwezbmJvlV4_sxvK6x3hU-Rp4130_provenance
{
dgn-np:NP144569.RAZDX59RV99nvHsz9J3rfwezbmJvlV4_sxvK6x3hU-Rp4130_assertion
dcterms:description
"[loss of expression of MGMT occurs more frequently in cancer than in adenoma in both sporadic and familial adenomatous polyposis patients, and loss of expression of MGMT is associated with hypermethylation of the promoter area of MGMT gene.]. 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:12720298
;
prov:wasDerivedFrom
dgn-void:lhgdn-20090331
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:lhgdn-20090331
pav:importedOn
"2009-03-31"^^
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:NP144569.RAZDX59RV99nvHsz9J3rfwezbmJvlV4_sxvK6x3hU-Rp4130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:15+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" .
}