@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP216541.RAc6TXgwA1lRdZAuruJeW6JfurL7MpZatsS33VoYQdyqQ
> .
@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:NP216541.RAc6TXgwA1lRdZAuruJeW6JfurL7MpZatsS33VoYQdyqQ130_head
{
this:
np:hasAssertion
dgn-np:NP216541.RAc6TXgwA1lRdZAuruJeW6JfurL7MpZatsS33VoYQdyqQ130_assertion
;
np:hasProvenance
dgn-np:NP216541.RAc6TXgwA1lRdZAuruJeW6JfurL7MpZatsS33VoYQdyqQ130_provenance
;
np:hasPublicationInfo
dgn-np:NP216541.RAc6TXgwA1lRdZAuruJeW6JfurL7MpZatsS33VoYQdyqQ130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP216541.RAc6TXgwA1lRdZAuruJeW6JfurL7MpZatsS33VoYQdyqQ130_assertion
a
np:Assertion
.
dgn-np:NP216541.RAc6TXgwA1lRdZAuruJeW6JfurL7MpZatsS33VoYQdyqQ130_provenance
a
np:Provenance
.
dgn-np:NP216541.RAc6TXgwA1lRdZAuruJeW6JfurL7MpZatsS33VoYQdyqQ130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP216541.RAc6TXgwA1lRdZAuruJeW6JfurL7MpZatsS33VoYQdyqQ130_assertion
{
miriam-gene:283120
a
ncit:C16612
.
lld:C0205851
a
ncit:C7057
.
dgn-gda:DGN5595e7be50ec9e2715392c10b6ca834e
sio:SIO_000628
miriam-gene:283120
,
lld:C0205851
;
a
sio:SIO_001121
.
}
dgn-np:NP216541.RAc6TXgwA1lRdZAuruJeW6JfurL7MpZatsS33VoYQdyqQ130_provenance
{
dgn-np:NP216541.RAc6TXgwA1lRdZAuruJeW6JfurL7MpZatsS33VoYQdyqQ130_assertion
dcterms:description
"[To explore the mechanisms of GCT formation, we analyzed single-nucleotide polymorphism array comparative genomic hybridization patterns and the methylation status of 15 tumor suppressor genes (TSGs) and differentially methylated regions (DMRs) of two imprinted genes, H19 and SNRPN, in 28 children with GCTs.]. 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:23225212
;
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:NP216541.RAc6TXgwA1lRdZAuruJeW6JfurL7MpZatsS33VoYQdyqQ130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:00+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" .
}