@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP156016.RA260JwNo8frOQa-jYOtgSpnjtiFl5rPSl39Ij3KQ_odI
> .
@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:NP156016.RA260JwNo8frOQa-jYOtgSpnjtiFl5rPSl39Ij3KQ_odI130_head
{
this:
np:hasAssertion
dgn-np:NP156016.RA260JwNo8frOQa-jYOtgSpnjtiFl5rPSl39Ij3KQ_odI130_assertion
;
np:hasProvenance
dgn-np:NP156016.RA260JwNo8frOQa-jYOtgSpnjtiFl5rPSl39Ij3KQ_odI130_provenance
;
np:hasPublicationInfo
dgn-np:NP156016.RA260JwNo8frOQa-jYOtgSpnjtiFl5rPSl39Ij3KQ_odI130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP156016.RA260JwNo8frOQa-jYOtgSpnjtiFl5rPSl39Ij3KQ_odI130_assertion
a
np:Assertion
.
dgn-np:NP156016.RA260JwNo8frOQa-jYOtgSpnjtiFl5rPSl39Ij3KQ_odI130_provenance
a
np:Provenance
.
dgn-np:NP156016.RA260JwNo8frOQa-jYOtgSpnjtiFl5rPSl39Ij3KQ_odI130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP156016.RA260JwNo8frOQa-jYOtgSpnjtiFl5rPSl39Ij3KQ_odI130_assertion
{
miriam-gene:7157
a
ncit:C16612
.
lld:C0017638
a
ncit:C7057
.
dgn-gda:DGNe340c22c73305fad4626e0568a9d7358
sio:SIO_000628
miriam-gene:7157
,
lld:C0017638
;
a
sio:SIO_001121
.
}
dgn-np:NP156016.RA260JwNo8frOQa-jYOtgSpnjtiFl5rPSl39Ij3KQ_odI130_provenance
{
dgn-np:NP156016.RA260JwNo8frOQa-jYOtgSpnjtiFl5rPSl39Ij3KQ_odI130_assertion
dcterms:description
"[The earliest events of glioma progression include loss of genetic information from the long arms of chromosomes 13 or 22, or the short arm of chromosome 17 for which targeting of the TP53 (p53) gene has been indicated.]. 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:8344489
;
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:NP156016.RA260JwNo8frOQa-jYOtgSpnjtiFl5rPSl39Ij3KQ_odI130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:24+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" .
}