@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP422772.RAzUNGrt5u2m8XHm9KuYqNY03208Vb9IGthzbojdO6N-I
> .
@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:NP422772.RAzUNGrt5u2m8XHm9KuYqNY03208Vb9IGthzbojdO6N-I130_head
{
this:
np:hasAssertion
dgn-np:NP422772.RAzUNGrt5u2m8XHm9KuYqNY03208Vb9IGthzbojdO6N-I130_assertion
;
np:hasProvenance
dgn-np:NP422772.RAzUNGrt5u2m8XHm9KuYqNY03208Vb9IGthzbojdO6N-I130_provenance
;
np:hasPublicationInfo
dgn-np:NP422772.RAzUNGrt5u2m8XHm9KuYqNY03208Vb9IGthzbojdO6N-I130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP422772.RAzUNGrt5u2m8XHm9KuYqNY03208Vb9IGthzbojdO6N-I130_assertion
a
np:Assertion
.
dgn-np:NP422772.RAzUNGrt5u2m8XHm9KuYqNY03208Vb9IGthzbojdO6N-I130_provenance
a
np:Provenance
.
dgn-np:NP422772.RAzUNGrt5u2m8XHm9KuYqNY03208Vb9IGthzbojdO6N-I130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP422772.RAzUNGrt5u2m8XHm9KuYqNY03208Vb9IGthzbojdO6N-I130_assertion
{
miriam-gene:7157
a
ncit:C16612
.
lld:C0027766
a
ncit:C7057
.
dgn-gda:DGNd5e7ef40dca6a05f58974eb15d4c7b97
sio:SIO_000628
miriam-gene:7157
,
lld:C0027766
;
a
sio:SIO_001121
.
}
dgn-np:NP422772.RAzUNGrt5u2m8XHm9KuYqNY03208Vb9IGthzbojdO6N-I130_provenance
{
dgn-np:NP422772.RAzUNGrt5u2m8XHm9KuYqNY03208Vb9IGthzbojdO6N-I130_assertion
dcterms:description
"[To determine the relevance of defective MGMT function due to aberrant methylation in relation to the presence of TP53 mutations, we studied 469 nervous system tumors (including all major histological subtypes) for MGMT promoter methylation and TP53 mutations at exons 5-8.]. 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:15450401
;
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:NP422772.RAzUNGrt5u2m8XHm9KuYqNY03208Vb9IGthzbojdO6N-I130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:11+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" .
}