@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP219456.RAMOFI8ypwha5Gn6frE-DJLlBCEz1fN3rgM-Suo1U9UfA
> .
@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:NP219456.RAMOFI8ypwha5Gn6frE-DJLlBCEz1fN3rgM-Suo1U9UfA130_head
{
this:
np:hasAssertion
dgn-np:NP219456.RAMOFI8ypwha5Gn6frE-DJLlBCEz1fN3rgM-Suo1U9UfA130_assertion
;
np:hasProvenance
dgn-np:NP219456.RAMOFI8ypwha5Gn6frE-DJLlBCEz1fN3rgM-Suo1U9UfA130_provenance
;
np:hasPublicationInfo
dgn-np:NP219456.RAMOFI8ypwha5Gn6frE-DJLlBCEz1fN3rgM-Suo1U9UfA130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP219456.RAMOFI8ypwha5Gn6frE-DJLlBCEz1fN3rgM-Suo1U9UfA130_assertion
a
np:Assertion
.
dgn-np:NP219456.RAMOFI8ypwha5Gn6frE-DJLlBCEz1fN3rgM-Suo1U9UfA130_provenance
a
np:Provenance
.
dgn-np:NP219456.RAMOFI8ypwha5Gn6frE-DJLlBCEz1fN3rgM-Suo1U9UfA130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP219456.RAMOFI8ypwha5Gn6frE-DJLlBCEz1fN3rgM-Suo1U9UfA130_assertion
{
miriam-gene:1788
a
ncit:C16612
.
lld:C0043117
a
ncit:C7057
.
dgn-gda:DGNb5fbecfa5c6f3d17896ad8663a7c4274
sio:SIO_000628
miriam-gene:1788
,
lld:C0043117
;
a
sio:SIO_001121
.
}
dgn-np:NP219456.RAMOFI8ypwha5Gn6frE-DJLlBCEz1fN3rgM-Suo1U9UfA130_provenance
{
dgn-np:NP219456.RAMOFI8ypwha5Gn6frE-DJLlBCEz1fN3rgM-Suo1U9UfA130_assertion
dcterms:description
"[Our observations suggest that aberrant DNA methylation status reflected by increased plasma SAH concentration and decreased mRNA expression levels of DNMT3A and 3B are possibly involved in the pathogenesis of ITP although the precise mechanisms need further study.]. 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:18683034
;
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:NP219456.RAMOFI8ypwha5Gn6frE-DJLlBCEz1fN3rgM-Suo1U9UfA130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:01+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" .
}