@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP191288.RAc-tkTZVUtzHPVlhjI6z08xuyqQkLhfsUU39b4x8XXkM
> .
@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:NP191288.RAc-tkTZVUtzHPVlhjI6z08xuyqQkLhfsUU39b4x8XXkM130_head
{
this:
np:hasAssertion
dgn-np:NP191288.RAc-tkTZVUtzHPVlhjI6z08xuyqQkLhfsUU39b4x8XXkM130_assertion
;
np:hasProvenance
dgn-np:NP191288.RAc-tkTZVUtzHPVlhjI6z08xuyqQkLhfsUU39b4x8XXkM130_provenance
;
np:hasPublicationInfo
dgn-np:NP191288.RAc-tkTZVUtzHPVlhjI6z08xuyqQkLhfsUU39b4x8XXkM130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP191288.RAc-tkTZVUtzHPVlhjI6z08xuyqQkLhfsUU39b4x8XXkM130_assertion
a
np:Assertion
.
dgn-np:NP191288.RAc-tkTZVUtzHPVlhjI6z08xuyqQkLhfsUU39b4x8XXkM130_provenance
a
np:Provenance
.
dgn-np:NP191288.RAc-tkTZVUtzHPVlhjI6z08xuyqQkLhfsUU39b4x8XXkM130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP191288.RAc-tkTZVUtzHPVlhjI6z08xuyqQkLhfsUU39b4x8XXkM130_assertion
{
miriam-gene:1571
a
ncit:C16612
.
lld:C0030567
a
ncit:C7057
.
dgn-gda:DGN1b5b19a23597d536d76109a19254f07e
sio:SIO_000628
miriam-gene:1571
,
lld:C0030567
;
a
sio:SIO_001121
.
}
dgn-np:NP191288.RAc-tkTZVUtzHPVlhjI6z08xuyqQkLhfsUU39b4x8XXkM130_provenance
{
dgn-np:NP191288.RAc-tkTZVUtzHPVlhjI6z08xuyqQkLhfsUU39b4x8XXkM130_assertion
dcterms:description
"[The list of ME candidates exhibited overlaps with recently identified human genes (including CYP2E1 and MGMT, where methylation has been associated with Parkinson disease and glioblastoma, respectively) in which perinatal DNA methylation levels where linked to maternal periconceptual nutrition.]. 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:23321599
;
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:NP191288.RAc-tkTZVUtzHPVlhjI6z08xuyqQkLhfsUU39b4x8XXkM130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:45+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" .
}