@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP460961.RAPdTC6lf0JwPzaStBLHmU60P8vX9atS0gOTw2p2Bb8VQ
> .
@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:NP460961.RAPdTC6lf0JwPzaStBLHmU60P8vX9atS0gOTw2p2Bb8VQ130_head
{
this:
np:hasAssertion
dgn-np:NP460961.RAPdTC6lf0JwPzaStBLHmU60P8vX9atS0gOTw2p2Bb8VQ130_assertion
;
np:hasProvenance
dgn-np:NP460961.RAPdTC6lf0JwPzaStBLHmU60P8vX9atS0gOTw2p2Bb8VQ130_provenance
;
np:hasPublicationInfo
dgn-np:NP460961.RAPdTC6lf0JwPzaStBLHmU60P8vX9atS0gOTw2p2Bb8VQ130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP460961.RAPdTC6lf0JwPzaStBLHmU60P8vX9atS0gOTw2p2Bb8VQ130_assertion
a
np:Assertion
.
dgn-np:NP460961.RAPdTC6lf0JwPzaStBLHmU60P8vX9atS0gOTw2p2Bb8VQ130_provenance
a
np:Provenance
.
dgn-np:NP460961.RAPdTC6lf0JwPzaStBLHmU60P8vX9atS0gOTw2p2Bb8VQ130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP460961.RAPdTC6lf0JwPzaStBLHmU60P8vX9atS0gOTw2p2Bb8VQ130_assertion
{
miriam-gene:3351
a
ncit:C16612
.
lld:C0267244
a
ncit:C7057
.
dgn-gda:DGN8e76d95a81d24b96b66c57bc73c49737
sio:SIO_000628
miriam-gene:3351
,
lld:C0267244
;
a
sio:SIO_001121
.
}
dgn-np:NP460961.RAPdTC6lf0JwPzaStBLHmU60P8vX9atS0gOTw2p2Bb8VQ130_provenance
{
dgn-np:NP460961.RAPdTC6lf0JwPzaStBLHmU60P8vX9atS0gOTw2p2Bb8VQ130_assertion
dcterms:description
"[MS-RDA was shown to isolate DNA fragments that are hypermethylated and silenced, such as HTR1B, and those whose expressions are altered and the methylation statuses outside the promoter region are altered, such as EDN1.]. 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:11709722
;
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:NP460961.RAPdTC6lf0JwPzaStBLHmU60P8vX9atS0gOTw2p2Bb8VQ130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:34+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" .
}