@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP614115.RAIkj2HdP5K7Oy--o2Dlq4Odat-CfYm0w4fqatVQgKw_0
> .
@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:NP614115.RAIkj2HdP5K7Oy--o2Dlq4Odat-CfYm0w4fqatVQgKw_0130_head
{
this:
np:hasAssertion
dgn-np:NP614115.RAIkj2HdP5K7Oy--o2Dlq4Odat-CfYm0w4fqatVQgKw_0130_assertion
;
np:hasProvenance
dgn-np:NP614115.RAIkj2HdP5K7Oy--o2Dlq4Odat-CfYm0w4fqatVQgKw_0130_provenance
;
np:hasPublicationInfo
dgn-np:NP614115.RAIkj2HdP5K7Oy--o2Dlq4Odat-CfYm0w4fqatVQgKw_0130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP614115.RAIkj2HdP5K7Oy--o2Dlq4Odat-CfYm0w4fqatVQgKw_0130_assertion
a
np:Assertion
.
dgn-np:NP614115.RAIkj2HdP5K7Oy--o2Dlq4Odat-CfYm0w4fqatVQgKw_0130_provenance
a
np:Provenance
.
dgn-np:NP614115.RAIkj2HdP5K7Oy--o2Dlq4Odat-CfYm0w4fqatVQgKw_0130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP614115.RAIkj2HdP5K7Oy--o2Dlq4Odat-CfYm0w4fqatVQgKw_0130_assertion
{
miriam-gene:1124
a
ncit:C16612
.
lld:C0279626
a
ncit:C7057
.
dgn-gda:DGN04c3efed1c4259574ffcdcc64567a421
sio:SIO_000628
miriam-gene:1124
,
lld:C0279626
;
a
sio:SIO_001121
.
}
dgn-np:NP614115.RAIkj2HdP5K7Oy--o2Dlq4Odat-CfYm0w4fqatVQgKw_0130_provenance
{
dgn-np:NP614115.RAIkj2HdP5K7Oy--o2Dlq4Odat-CfYm0w4fqatVQgKw_0130_assertion
dcterms:description
"[The frequency of the loss of MGMT mRNA and protein expression progressively decreased from normal to BCH, DYS, and ESCC, and it was highly correlated with MGMT promoter hypermethylation according to Fisher's exact tests.]. 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:15703815
;
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:NP614115.RAIkj2HdP5K7Oy--o2Dlq4Odat-CfYm0w4fqatVQgKw_0130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:11+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" .
}