@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP351928.RA0eJoCGRtz3wiDCtKZGEYYALLPjpqJ9VfNybx1pn_FEY
> .
@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:NP351928.RA0eJoCGRtz3wiDCtKZGEYYALLPjpqJ9VfNybx1pn_FEY130_head
{
this:
np:hasAssertion
dgn-np:NP351928.RA0eJoCGRtz3wiDCtKZGEYYALLPjpqJ9VfNybx1pn_FEY130_assertion
;
np:hasProvenance
dgn-np:NP351928.RA0eJoCGRtz3wiDCtKZGEYYALLPjpqJ9VfNybx1pn_FEY130_provenance
;
np:hasPublicationInfo
dgn-np:NP351928.RA0eJoCGRtz3wiDCtKZGEYYALLPjpqJ9VfNybx1pn_FEY130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP351928.RA0eJoCGRtz3wiDCtKZGEYYALLPjpqJ9VfNybx1pn_FEY130_assertion
a
np:Assertion
.
dgn-np:NP351928.RA0eJoCGRtz3wiDCtKZGEYYALLPjpqJ9VfNybx1pn_FEY130_provenance
a
np:Provenance
.
dgn-np:NP351928.RA0eJoCGRtz3wiDCtKZGEYYALLPjpqJ9VfNybx1pn_FEY130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP351928.RA0eJoCGRtz3wiDCtKZGEYYALLPjpqJ9VfNybx1pn_FEY130_assertion
{
miriam-gene:83478
a
ncit:C16612
.
lld:C1762616
a
ncit:C7057
.
dgn-gda:DGN593c7710cb1e49bc8c70647d6579587f
sio:SIO_000628
miriam-gene:83478
,
lld:C1762616
;
a
sio:SIO_001121
.
}
dgn-np:NP351928.RA0eJoCGRtz3wiDCtKZGEYYALLPjpqJ9VfNybx1pn_FEY130_provenance
{
dgn-np:NP351928.RA0eJoCGRtz3wiDCtKZGEYYALLPjpqJ9VfNybx1pn_FEY130_assertion
dcterms:description
"[The aim of this study was to identify genes related to meningioma progression from the benign state to the atypical and anaplastic states by examining 1p LOH and the promoter methylation of RASSF1A and p73.]. 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:17695396
;
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:NP351928.RA0eJoCGRtz3wiDCtKZGEYYALLPjpqJ9VfNybx1pn_FEY130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:26+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" .
}