@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP655195.RA6nAmj9eE8O2Bok_OFClvgqHUjkpeTwXlfT3KIk8k9j4
> .
@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/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@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/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v3.0.0/void/
> .
dgn-np:NP655195.RA6nAmj9eE8O2Bok_OFClvgqHUjkpeTwXlfT3KIk8k9j4130_head
{
this:
np:hasAssertion
dgn-np:NP655195.RA6nAmj9eE8O2Bok_OFClvgqHUjkpeTwXlfT3KIk8k9j4130_assertion
;
np:hasProvenance
dgn-np:NP655195.RA6nAmj9eE8O2Bok_OFClvgqHUjkpeTwXlfT3KIk8k9j4130_provenance
;
np:hasPublicationInfo
dgn-np:NP655195.RA6nAmj9eE8O2Bok_OFClvgqHUjkpeTwXlfT3KIk8k9j4130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP655195.RA6nAmj9eE8O2Bok_OFClvgqHUjkpeTwXlfT3KIk8k9j4130_assertion
a
np:Assertion
.
dgn-np:NP655195.RA6nAmj9eE8O2Bok_OFClvgqHUjkpeTwXlfT3KIk8k9j4130_provenance
a
np:Provenance
.
dgn-np:NP655195.RA6nAmj9eE8O2Bok_OFClvgqHUjkpeTwXlfT3KIk8k9j4130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP655195.RA6nAmj9eE8O2Bok_OFClvgqHUjkpeTwXlfT3KIk8k9j4130_assertion
{
miriam-gene:5728
a
ncit:C16612
.
lld:C2939419
a
ncit:C7057
.
dgn-gda:DGN5eb2e068fce36022acf0f81af220d4ed
sio:SIO_000628
miriam-gene:5728
,
lld:C2939419
;
a
sio:SIO_001121
.
}
dgn-np:NP655195.RA6nAmj9eE8O2Bok_OFClvgqHUjkpeTwXlfT3KIk8k9j4130_provenance
{
dgn-np:NP655195.RA6nAmj9eE8O2Bok_OFClvgqHUjkpeTwXlfT3KIk8k9j4130_assertion
dcterms:description
"[Detection of certain molecular markers such as deletion of 1p and 19q chromosomal arms, hypermethylation of MGMT promoter, and characteristic PTEN exon mutations may help differentiate subtypes which are more prone to extracranial metastases.]. 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:24447608
;
prov:wasDerivedFrom
dgn-void:befree-20150227
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-20150227
pav:importedOn
"2015-02-27"^^
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:NP655195.RA6nAmj9eE8O2Bok_OFClvgqHUjkpeTwXlfT3KIk8k9j4130_publicationInfo
{
this:
dcterms:created
"2015-08-25T14:44:13+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:disgenetv3.0rdf
;
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
"v3.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v3.0.0" .
}