@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP297178.RAwXUpCcddM2F8unXOVRDt_UUfKiXOqHayOYKkUo7BZ2E
> .
@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:NP297178.RAwXUpCcddM2F8unXOVRDt_UUfKiXOqHayOYKkUo7BZ2E130_head
{
this:
np:hasAssertion
dgn-np:NP297178.RAwXUpCcddM2F8unXOVRDt_UUfKiXOqHayOYKkUo7BZ2E130_assertion
;
np:hasProvenance
dgn-np:NP297178.RAwXUpCcddM2F8unXOVRDt_UUfKiXOqHayOYKkUo7BZ2E130_provenance
;
np:hasPublicationInfo
dgn-np:NP297178.RAwXUpCcddM2F8unXOVRDt_UUfKiXOqHayOYKkUo7BZ2E130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP297178.RAwXUpCcddM2F8unXOVRDt_UUfKiXOqHayOYKkUo7BZ2E130_assertion
a
np:Assertion
.
dgn-np:NP297178.RAwXUpCcddM2F8unXOVRDt_UUfKiXOqHayOYKkUo7BZ2E130_provenance
a
np:Provenance
.
dgn-np:NP297178.RAwXUpCcddM2F8unXOVRDt_UUfKiXOqHayOYKkUo7BZ2E130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP297178.RAwXUpCcddM2F8unXOVRDt_UUfKiXOqHayOYKkUo7BZ2E130_assertion
{
miriam-gene:5243
a
ncit:C16612
.
lld:C0854467
a
ncit:C7057
.
dgn-gda:DGN8998196c6571356432376c61bec884ef
sio:SIO_000628
miriam-gene:5243
,
lld:C0854467
;
a
sio:SIO_001121
.
}
dgn-np:NP297178.RAwXUpCcddM2F8unXOVRDt_UUfKiXOqHayOYKkUo7BZ2E130_provenance
{
dgn-np:NP297178.RAwXUpCcddM2F8unXOVRDt_UUfKiXOqHayOYKkUo7BZ2E130_assertion
dcterms:description
"[DNA was extracted from the patients' mononuclear cells and genotyping of O-methylguanine-DNA-methyltransferase (MGMT), multidrug resistance (MDR1; also known as ABCB1), NQO1, and GSTP1 genes and analysis for the epigenetic silencing of specific MGMT gene promoters were carried out to evaluate the possible genetic determinants of increased risk of severe TMZ-induced myelosuppression.]. 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:20938339
;
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:NP297178.RAwXUpCcddM2F8unXOVRDt_UUfKiXOqHayOYKkUo7BZ2E130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:49+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" .
}