@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP239304.RA0FoQ-e82Eiybg92gKgEHxUw3gGcrhXBbp8S3qfkoIlY
> .
@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:NP239304.RA0FoQ-e82Eiybg92gKgEHxUw3gGcrhXBbp8S3qfkoIlY130_head
{
this:
np:hasAssertion
dgn-np:NP239304.RA0FoQ-e82Eiybg92gKgEHxUw3gGcrhXBbp8S3qfkoIlY130_assertion
;
np:hasProvenance
dgn-np:NP239304.RA0FoQ-e82Eiybg92gKgEHxUw3gGcrhXBbp8S3qfkoIlY130_provenance
;
np:hasPublicationInfo
dgn-np:NP239304.RA0FoQ-e82Eiybg92gKgEHxUw3gGcrhXBbp8S3qfkoIlY130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP239304.RA0FoQ-e82Eiybg92gKgEHxUw3gGcrhXBbp8S3qfkoIlY130_assertion
a
np:Assertion
.
dgn-np:NP239304.RA0FoQ-e82Eiybg92gKgEHxUw3gGcrhXBbp8S3qfkoIlY130_provenance
a
np:Provenance
.
dgn-np:NP239304.RA0FoQ-e82Eiybg92gKgEHxUw3gGcrhXBbp8S3qfkoIlY130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP239304.RA0FoQ-e82Eiybg92gKgEHxUw3gGcrhXBbp8S3qfkoIlY130_assertion
{
miriam-gene:1017
a
ncit:C16612
.
lld:C0206663
a
ncit:C7057
.
dgn-gda:DGN8bc14ed852e2d9bdba30b39b4d948550
sio:SIO_000628
miriam-gene:1017
,
lld:C0206663
;
a
sio:SIO_001121
.
}
dgn-np:NP239304.RA0FoQ-e82Eiybg92gKgEHxUw3gGcrhXBbp8S3qfkoIlY130_provenance
{
dgn-np:NP239304.RA0FoQ-e82Eiybg92gKgEHxUw3gGcrhXBbp8S3qfkoIlY130_assertion
dcterms:description
"[To investigate the possible role of this gene in the genesis of the central nervous system primitive neuroectodermal tumor (PNET), four established PNET cell lines and 18 PNET surgical specimens were studied for deletions and mutations of the MTS1/CDKN2 gene.]. 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:7791990
;
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:NP239304.RA0FoQ-e82Eiybg92gKgEHxUw3gGcrhXBbp8S3qfkoIlY130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:14+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" .
}