@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP610883.RAoC5tAbVfSwMFFV1qLhV2J91iguL178Tab9UEjB1qhSI
> .
@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:NP610883.RAoC5tAbVfSwMFFV1qLhV2J91iguL178Tab9UEjB1qhSI130_head
{
this:
np:hasAssertion
dgn-np:NP610883.RAoC5tAbVfSwMFFV1qLhV2J91iguL178Tab9UEjB1qhSI130_assertion
;
np:hasProvenance
dgn-np:NP610883.RAoC5tAbVfSwMFFV1qLhV2J91iguL178Tab9UEjB1qhSI130_provenance
;
np:hasPublicationInfo
dgn-np:NP610883.RAoC5tAbVfSwMFFV1qLhV2J91iguL178Tab9UEjB1qhSI130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP610883.RAoC5tAbVfSwMFFV1qLhV2J91iguL178Tab9UEjB1qhSI130_assertion
a
np:Assertion
.
dgn-np:NP610883.RAoC5tAbVfSwMFFV1qLhV2J91iguL178Tab9UEjB1qhSI130_provenance
a
np:Provenance
.
dgn-np:NP610883.RAoC5tAbVfSwMFFV1qLhV2J91iguL178Tab9UEjB1qhSI130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP610883.RAoC5tAbVfSwMFFV1qLhV2J91iguL178Tab9UEjB1qhSI130_assertion
{
miriam-gene:1956
a
ncit:C16612
.
lld:C0028945
a
ncit:C7057
.
dgn-gda:DGN5cab46e1b80d207cc28b5a325e424f52
sio:SIO_000628
miriam-gene:1956
,
lld:C0028945
;
a
sio:SIO_001121
.
}
dgn-np:NP610883.RAoC5tAbVfSwMFFV1qLhV2J91iguL178Tab9UEjB1qhSI130_provenance
{
dgn-np:NP610883.RAoC5tAbVfSwMFFV1qLhV2J91iguL178Tab9UEjB1qhSI130_assertion
dcterms:description
"[The study analysed INA, nestin, Olig2 and p53 expression, loss of heterozygosity of microsatellite markers from telomere to centromere of 10p, 10q, 1p and 19q chromosomes and epidermal growth factor receptor gene (EGFR) amplification in 40 gliomas (five astrocytomas, 12 oligodendrogliomas, 11 oligoastrocytomas, 12 glioblastomas).]. 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:21653654
;
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:NP610883.RAoC5tAbVfSwMFFV1qLhV2J91iguL178Tab9UEjB1qhSI130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:09+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" .
}