@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP563597.RABOxbuIKavXNhl64LwT33PFEV0YkVe06BUC7xgBR3vM4
> .
@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:NP563597.RABOxbuIKavXNhl64LwT33PFEV0YkVe06BUC7xgBR3vM4130_head
{
this:
np:hasAssertion
dgn-np:NP563597.RABOxbuIKavXNhl64LwT33PFEV0YkVe06BUC7xgBR3vM4130_assertion
;
np:hasProvenance
dgn-np:NP563597.RABOxbuIKavXNhl64LwT33PFEV0YkVe06BUC7xgBR3vM4130_provenance
;
np:hasPublicationInfo
dgn-np:NP563597.RABOxbuIKavXNhl64LwT33PFEV0YkVe06BUC7xgBR3vM4130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP563597.RABOxbuIKavXNhl64LwT33PFEV0YkVe06BUC7xgBR3vM4130_assertion
a
np:Assertion
.
dgn-np:NP563597.RABOxbuIKavXNhl64LwT33PFEV0YkVe06BUC7xgBR3vM4130_provenance
a
np:Provenance
.
dgn-np:NP563597.RABOxbuIKavXNhl64LwT33PFEV0YkVe06BUC7xgBR3vM4130_publicationInfo
a
np:PublicationInfo
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dgn-np:NP563597.RABOxbuIKavXNhl64LwT33PFEV0YkVe06BUC7xgBR3vM4130_assertion
{
miriam-gene:7157
a
ncit:C16612
.
lld:C0280785
a
ncit:C7057
.
dgn-gda:DGN5f707cb8c1219274f96273335e1092fb
sio:SIO_000628
miriam-gene:7157
,
lld:C0280785
;
a
sio:SIO_001121
.
}
dgn-np:NP563597.RABOxbuIKavXNhl64LwT33PFEV0YkVe06BUC7xgBR3vM4130_provenance
{
dgn-np:NP563597.RABOxbuIKavXNhl64LwT33PFEV0YkVe06BUC7xgBR3vM4130_assertion
dcterms:description
"[We had previously reported that loss of heterozygosity (LOH) of the D17S379 locus on 17p13.3 was significantly more frequent in high-grade gliomas (anaplastic astrocytoma, AA; glioblastoma multiforme, GBM) than in those of a low-grade diffuse astrocytoma (DA); however, this was independent of alterations at the TP53 locus, We also showed that LOH of D17S379 was associated with positive staining for p53 protein on immunohistochemistry, but LOH of the TP53 gene had no such association.]. 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:12850379
;
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:NP563597.RABOxbuIKavXNhl64LwT33PFEV0YkVe06BUC7xgBR3vM4130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:39+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
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dgn-void:disgenetrdf
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