@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP656743.RArqMoTmZAJReoIDX1zCNWv_uQBea_KgtibH9HniGrl3A
> .
@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:NP656743.RArqMoTmZAJReoIDX1zCNWv_uQBea_KgtibH9HniGrl3A130_head
{
this:
np:hasAssertion
dgn-np:NP656743.RArqMoTmZAJReoIDX1zCNWv_uQBea_KgtibH9HniGrl3A130_assertion
;
np:hasProvenance
dgn-np:NP656743.RArqMoTmZAJReoIDX1zCNWv_uQBea_KgtibH9HniGrl3A130_provenance
;
np:hasPublicationInfo
dgn-np:NP656743.RArqMoTmZAJReoIDX1zCNWv_uQBea_KgtibH9HniGrl3A130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP656743.RArqMoTmZAJReoIDX1zCNWv_uQBea_KgtibH9HniGrl3A130_assertion
a
np:Assertion
.
dgn-np:NP656743.RArqMoTmZAJReoIDX1zCNWv_uQBea_KgtibH9HniGrl3A130_provenance
a
np:Provenance
.
dgn-np:NP656743.RArqMoTmZAJReoIDX1zCNWv_uQBea_KgtibH9HniGrl3A130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP656743.RArqMoTmZAJReoIDX1zCNWv_uQBea_KgtibH9HniGrl3A130_assertion
{
miriam-gene:1788
a
ncit:C16612
.
lld:C0043117
a
ncit:C7057
.
dgn-gda:DGN1ea71bcc740fcc8635f523d5f773bb0e
sio:SIO_000628
miriam-gene:1788
,
lld:C0043117
;
a
sio:SIO_001121
.
}
dgn-np:NP656743.RArqMoTmZAJReoIDX1zCNWv_uQBea_KgtibH9HniGrl3A130_provenance
{
dgn-np:NP656743.RArqMoTmZAJReoIDX1zCNWv_uQBea_KgtibH9HniGrl3A130_assertion
dcterms:description
"[Conclusions: Aberrant DNA methylation status reflected by decreased mRNA expression of DNMT3A and increased plasma SAH level may play an important role in the pathogenesis of ITP, although the precise underlying mechanisms still await further investigations, and extensive work in this field is clearly needed to provide novel therapeutic targets for ITP.]. 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:22321265
;
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:NP656743.RArqMoTmZAJReoIDX1zCNWv_uQBea_KgtibH9HniGrl3A130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:35+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" .
}