@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP671843.RAHvCDWbuhxhvetF0I52G2TFcOxrvLA2_St1GOqS2vSF0
> .
@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:NP671843.RAHvCDWbuhxhvetF0I52G2TFcOxrvLA2_St1GOqS2vSF0130_head
{
this:
np:hasAssertion
dgn-np:NP671843.RAHvCDWbuhxhvetF0I52G2TFcOxrvLA2_St1GOqS2vSF0130_assertion
;
np:hasProvenance
dgn-np:NP671843.RAHvCDWbuhxhvetF0I52G2TFcOxrvLA2_St1GOqS2vSF0130_provenance
;
np:hasPublicationInfo
dgn-np:NP671843.RAHvCDWbuhxhvetF0I52G2TFcOxrvLA2_St1GOqS2vSF0130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP671843.RAHvCDWbuhxhvetF0I52G2TFcOxrvLA2_St1GOqS2vSF0130_assertion
a
np:Assertion
.
dgn-np:NP671843.RAHvCDWbuhxhvetF0I52G2TFcOxrvLA2_St1GOqS2vSF0130_provenance
a
np:Provenance
.
dgn-np:NP671843.RAHvCDWbuhxhvetF0I52G2TFcOxrvLA2_St1GOqS2vSF0130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP671843.RAHvCDWbuhxhvetF0I52G2TFcOxrvLA2_St1GOqS2vSF0130_assertion
{
miriam-gene:4397
a
ncit:C16612
.
lld:C0002736
a
ncit:C7057
.
dgn-gda:DGNea8e6c03fe5df872cd4552ff710fb15b
sio:SIO_000628
miriam-gene:4397
,
lld:C0002736
;
a
sio:SIO_001121
.
}
dgn-np:NP671843.RAHvCDWbuhxhvetF0I52G2TFcOxrvLA2_St1GOqS2vSF0130_provenance
{
dgn-np:NP671843.RAHvCDWbuhxhvetF0I52G2TFcOxrvLA2_St1GOqS2vSF0130_assertion
dcterms:description
"[Moreover, aberrant DNA methylation and histone modification profiles of discrete DNA sequences, and those at a genome-wide level, have just begun to be described for neurodegenerative disorders such as Alzheimer's disease, Parkinson's disease, and Huntington's disease, and in other neurological disorders such as multiple sclerosis, epilepsy, and amyotrophic lateral sclerosis.]. 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:19833297
;
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:NP671843.RAHvCDWbuhxhvetF0I52G2TFcOxrvLA2_St1GOqS2vSF0130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:45+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" .
}