@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP210234.RAST18F5wCZY8yI7tE4OtOgFd6sTnKDUsHIZHRD3OJTeg
> .
@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:NP210234.RAST18F5wCZY8yI7tE4OtOgFd6sTnKDUsHIZHRD3OJTeg130_head
{
this:
np:hasAssertion
dgn-np:NP210234.RAST18F5wCZY8yI7tE4OtOgFd6sTnKDUsHIZHRD3OJTeg130_assertion
;
np:hasProvenance
dgn-np:NP210234.RAST18F5wCZY8yI7tE4OtOgFd6sTnKDUsHIZHRD3OJTeg130_provenance
;
np:hasPublicationInfo
dgn-np:NP210234.RAST18F5wCZY8yI7tE4OtOgFd6sTnKDUsHIZHRD3OJTeg130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP210234.RAST18F5wCZY8yI7tE4OtOgFd6sTnKDUsHIZHRD3OJTeg130_assertion
a
np:Assertion
.
dgn-np:NP210234.RAST18F5wCZY8yI7tE4OtOgFd6sTnKDUsHIZHRD3OJTeg130_provenance
a
np:Provenance
.
dgn-np:NP210234.RAST18F5wCZY8yI7tE4OtOgFd6sTnKDUsHIZHRD3OJTeg130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP210234.RAST18F5wCZY8yI7tE4OtOgFd6sTnKDUsHIZHRD3OJTeg130_assertion
{
miriam-gene:3418
a
ncit:C16612
.
lld:C0017636
a
ncit:C7057
.
dgn-gda:DGNece50a5382d75d6a1a51aa81a21bd75b
sio:SIO_000628
miriam-gene:3418
,
lld:C0017636
;
a
sio:SIO_001121
.
}
dgn-np:NP210234.RAST18F5wCZY8yI7tE4OtOgFd6sTnKDUsHIZHRD3OJTeg130_provenance
{
dgn-np:NP210234.RAST18F5wCZY8yI7tE4OtOgFd6sTnKDUsHIZHRD3OJTeg130_assertion
dcterms:description
"[Based on this small series of sGBM patients treated with CRTx (concomitantly or sequentially) the frequency of PP appears to be very low in sGBM, even in those patients with methylated MGMT promoter or IDH mutations.]. 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:24267971
;
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:NP210234.RAST18F5wCZY8yI7tE4OtOgFd6sTnKDUsHIZHRD3OJTeg130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:56+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" .
}