@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP689981.RAK0ocXWxeF7WuIUUdrlKXw7L1IcH11fUhFWjBfR7ezQE
> .
@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:NP689981.RAK0ocXWxeF7WuIUUdrlKXw7L1IcH11fUhFWjBfR7ezQE130_head
{
this:
np:hasAssertion
dgn-np:NP689981.RAK0ocXWxeF7WuIUUdrlKXw7L1IcH11fUhFWjBfR7ezQE130_assertion
;
np:hasProvenance
dgn-np:NP689981.RAK0ocXWxeF7WuIUUdrlKXw7L1IcH11fUhFWjBfR7ezQE130_provenance
;
np:hasPublicationInfo
dgn-np:NP689981.RAK0ocXWxeF7WuIUUdrlKXw7L1IcH11fUhFWjBfR7ezQE130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP689981.RAK0ocXWxeF7WuIUUdrlKXw7L1IcH11fUhFWjBfR7ezQE130_assertion
a
np:Assertion
.
dgn-np:NP689981.RAK0ocXWxeF7WuIUUdrlKXw7L1IcH11fUhFWjBfR7ezQE130_provenance
a
np:Provenance
.
dgn-np:NP689981.RAK0ocXWxeF7WuIUUdrlKXw7L1IcH11fUhFWjBfR7ezQE130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP689981.RAK0ocXWxeF7WuIUUdrlKXw7L1IcH11fUhFWjBfR7ezQE130_assertion
{
miriam-gene:3205
a
ncit:C16612
.
lld:C1458156
a
ncit:C7057
.
dgn-gda:DGNcdfa7e15440499349008da1320ff1155
sio:SIO_000628
miriam-gene:3205
,
lld:C1458156
;
a
sio:SIO_001121
.
}
dgn-np:NP689981.RAK0ocXWxeF7WuIUUdrlKXw7L1IcH11fUhFWjBfR7ezQE130_provenance
{
dgn-np:NP689981.RAK0ocXWxeF7WuIUUdrlKXw7L1IcH11fUhFWjBfR7ezQE130_assertion
dcterms:description
"[Multivariate regression analyses showed that hypermethylation of these genes was an independent predictor of disease recurrence (HOXA9, ISL1 and ALDH1A3, either alone or in combination) and progression (ISL1 and ALDH1A3, either alone or in combination) (each p < 0.05).]. 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:23436614
;
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:NP689981.RAK0ocXWxeF7WuIUUdrlKXw7L1IcH11fUhFWjBfR7ezQE130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:59+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" .
}