@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP176119.RA4p7lsFpT5vi0S10sUjnFPdmR2rxDwSU5oPnxSmjNmXk
> .
@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:NP176119.RA4p7lsFpT5vi0S10sUjnFPdmR2rxDwSU5oPnxSmjNmXk130_head
{
this:
np:hasAssertion
dgn-np:NP176119.RA4p7lsFpT5vi0S10sUjnFPdmR2rxDwSU5oPnxSmjNmXk130_assertion
;
np:hasProvenance
dgn-np:NP176119.RA4p7lsFpT5vi0S10sUjnFPdmR2rxDwSU5oPnxSmjNmXk130_provenance
;
np:hasPublicationInfo
dgn-np:NP176119.RA4p7lsFpT5vi0S10sUjnFPdmR2rxDwSU5oPnxSmjNmXk130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP176119.RA4p7lsFpT5vi0S10sUjnFPdmR2rxDwSU5oPnxSmjNmXk130_assertion
a
np:Assertion
.
dgn-np:NP176119.RA4p7lsFpT5vi0S10sUjnFPdmR2rxDwSU5oPnxSmjNmXk130_provenance
a
np:Provenance
.
dgn-np:NP176119.RA4p7lsFpT5vi0S10sUjnFPdmR2rxDwSU5oPnxSmjNmXk130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP176119.RA4p7lsFpT5vi0S10sUjnFPdmR2rxDwSU5oPnxSmjNmXk130_assertion
{
miriam-gene:7157
a
ncit:C16612
.
lld:C0178874
a
ncit:C7057
.
dgn-gda:DGN483834329b01fe2d8633b7cfa5932b2c
sio:SIO_000628
miriam-gene:7157
,
lld:C0178874
;
a
sio:SIO_001121
.
}
dgn-np:NP176119.RA4p7lsFpT5vi0S10sUjnFPdmR2rxDwSU5oPnxSmjNmXk130_provenance
{
dgn-np:NP176119.RA4p7lsFpT5vi0S10sUjnFPdmR2rxDwSU5oPnxSmjNmXk130_assertion
dcterms:description
"[When compared with the histological grading, the rates of OS for Tel 17p and p53 in anaplastic astrocytomas were higher than those of glioblastomas, suggesting that the deletion may be associated with the early events in tumorigenesis and that some glioblastomas without chromosome 17 aberrations may be independent from tumour progression via low-grade gliomas.]. 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:7865231
;
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:NP176119.RA4p7lsFpT5vi0S10sUjnFPdmR2rxDwSU5oPnxSmjNmXk130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:35+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" .
}