@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP768047.RAalouFBCs5lZh4t0GKgJIJakKq8Z3_bmCvKdFZrbkY-k
> .
@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:NP768047.RAalouFBCs5lZh4t0GKgJIJakKq8Z3_bmCvKdFZrbkY-k130_head
{
this:
np:hasAssertion
dgn-np:NP768047.RAalouFBCs5lZh4t0GKgJIJakKq8Z3_bmCvKdFZrbkY-k130_assertion
;
np:hasProvenance
dgn-np:NP768047.RAalouFBCs5lZh4t0GKgJIJakKq8Z3_bmCvKdFZrbkY-k130_provenance
;
np:hasPublicationInfo
dgn-np:NP768047.RAalouFBCs5lZh4t0GKgJIJakKq8Z3_bmCvKdFZrbkY-k130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP768047.RAalouFBCs5lZh4t0GKgJIJakKq8Z3_bmCvKdFZrbkY-k130_assertion
a
np:Assertion
.
dgn-np:NP768047.RAalouFBCs5lZh4t0GKgJIJakKq8Z3_bmCvKdFZrbkY-k130_provenance
a
np:Provenance
.
dgn-np:NP768047.RAalouFBCs5lZh4t0GKgJIJakKq8Z3_bmCvKdFZrbkY-k130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP768047.RAalouFBCs5lZh4t0GKgJIJakKq8Z3_bmCvKdFZrbkY-k130_assertion
{
miriam-gene:2099
a
ncit:C16612
.
lld:C0004153
a
ncit:C7057
.
dgn-gda:DGNa2a5130c21923a59cac46903e64951a9
sio:SIO_000628
miriam-gene:2099
,
lld:C0004153
;
a
sio:SIO_001121
.
}
dgn-np:NP768047.RAalouFBCs5lZh4t0GKgJIJakKq8Z3_bmCvKdFZrbkY-k130_provenance
{
dgn-np:NP768047.RAalouFBCs5lZh4t0GKgJIJakKq8Z3_bmCvKdFZrbkY-k130_assertion
dcterms:description
"[Hypomethylation of genomic DNA is present in human atherosclerotic lesions and methylation changes also occur at the promoter level of several genes involved in the pathogenesis of atherosclerosis, such as extracellular superoxide dismutase, estrogen receptor-alpha, endothelial nitric oxide synthase and 15-lipoxygenase.]. 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:19233248
;
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:NP768047.RAalouFBCs5lZh4t0GKgJIJakKq8Z3_bmCvKdFZrbkY-k130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:45+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" .
}