@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP237729.RACJBvmAXa_8LEBHqrTXuc3ISaPr_vcdFYNpZftp0aubg
> .
@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/
> .
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{
this:
np:hasAssertion
dgn-np:NP237729.RACJBvmAXa_8LEBHqrTXuc3ISaPr_vcdFYNpZftp0aubg130_assertion
;
np:hasProvenance
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;
np:hasPublicationInfo
dgn-np:NP237729.RACJBvmAXa_8LEBHqrTXuc3ISaPr_vcdFYNpZftp0aubg130_publicationInfo
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a
np:Nanopublication
.
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a
np:Assertion
.
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a
np:Provenance
.
dgn-np:NP237729.RACJBvmAXa_8LEBHqrTXuc3ISaPr_vcdFYNpZftp0aubg130_publicationInfo
a
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.
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dgn-np:NP237729.RACJBvmAXa_8LEBHqrTXuc3ISaPr_vcdFYNpZftp0aubg130_assertion
{
miriam-gene:274
a
ncit:C16612
.
lld:C0002395
a
ncit:C7057
.
dgn-gda:DGN4673b5dc301df9ed820a8d540f6045af
sio:SIO_000628
miriam-gene:274
,
lld:C0002395
;
a
sio:SIO_001121
.
}
dgn-np:NP237729.RACJBvmAXa_8LEBHqrTXuc3ISaPr_vcdFYNpZftp0aubg130_provenance
{
dgn-np:NP237729.RACJBvmAXa_8LEBHqrTXuc3ISaPr_vcdFYNpZftp0aubg130_assertion
dcterms:description
"[We found that the level of methylation at 71 of the 415,848 interrogated CpGs was significantly associated with the burden of AD pathology, including CpGs in the ABCA7 and BIN1 regions, which harbor known AD susceptibility variants.]. 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:25129075
;
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:NP237729.RACJBvmAXa_8LEBHqrTXuc3ISaPr_vcdFYNpZftp0aubg130_publicationInfo
{
this:
dcterms:created
"2015-08-25T14:39:55+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
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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" .
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pav:version
"v3.0.0" .
}