@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP546359.RAulY1dtMn2XwXsYjgb2c-lkbpy4EYsNdT8z9Je9Px7bQ
> .
@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/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@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/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v3.0.0/void/
> .
dgn-np:NP546359.RAulY1dtMn2XwXsYjgb2c-lkbpy4EYsNdT8z9Je9Px7bQ130_head
{
this:
np:hasAssertion
dgn-np:NP546359.RAulY1dtMn2XwXsYjgb2c-lkbpy4EYsNdT8z9Je9Px7bQ130_assertion
;
np:hasProvenance
dgn-np:NP546359.RAulY1dtMn2XwXsYjgb2c-lkbpy4EYsNdT8z9Je9Px7bQ130_provenance
;
np:hasPublicationInfo
dgn-np:NP546359.RAulY1dtMn2XwXsYjgb2c-lkbpy4EYsNdT8z9Je9Px7bQ130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP546359.RAulY1dtMn2XwXsYjgb2c-lkbpy4EYsNdT8z9Je9Px7bQ130_assertion
a
np:Assertion
.
dgn-np:NP546359.RAulY1dtMn2XwXsYjgb2c-lkbpy4EYsNdT8z9Je9Px7bQ130_provenance
a
np:Provenance
.
dgn-np:NP546359.RAulY1dtMn2XwXsYjgb2c-lkbpy4EYsNdT8z9Je9Px7bQ130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP546359.RAulY1dtMn2XwXsYjgb2c-lkbpy4EYsNdT8z9Je9Px7bQ130_assertion
{
miriam-gene:4139
a
ncit:C16612
.
lld:C0006826
a
ncit:C7057
.
dgn-gda:DGN2867a183fcf4fa019c05f3b0c674468e
sio:SIO_000628
miriam-gene:4139
,
lld:C0006826
;
a
sio:SIO_001121
.
}
dgn-np:NP546359.RAulY1dtMn2XwXsYjgb2c-lkbpy4EYsNdT8z9Je9Px7bQ130_provenance
{
dgn-np:NP546359.RAulY1dtMn2XwXsYjgb2c-lkbpy4EYsNdT8z9Je9Px7bQ130_assertion
dcterms:description
"[Recently, however, it has been proposed that differential epigenetic variability may mark genes that contribute to the risk of complex genetic diseases like cancer and that identification of risk and early detection markers may therefore benefit from statistics based on differential variability.]. 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:22492641
;
prov:wasDerivedFrom
dgn-void:befree-20150227
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-20150227
pav:importedOn
"2015-02-27"^^
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:NP546359.RAulY1dtMn2XwXsYjgb2c-lkbpy4EYsNdT8z9Je9Px7bQ130_publicationInfo
{
this:
dcterms:created
"2015-08-25T14:43:03+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:disgenetv3.0rdf
;
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
"v3.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v3.0.0" .
}