@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP75852.RAvLNs9xXg7S419exdTn4AuUC-S5htGNyLR9VXlBzGwB8
> .
@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:NP75852.RAvLNs9xXg7S419exdTn4AuUC-S5htGNyLR9VXlBzGwB8130_head
{
this:
np:hasAssertion
dgn-np:NP75852.RAvLNs9xXg7S419exdTn4AuUC-S5htGNyLR9VXlBzGwB8130_assertion
;
np:hasProvenance
dgn-np:NP75852.RAvLNs9xXg7S419exdTn4AuUC-S5htGNyLR9VXlBzGwB8130_provenance
;
np:hasPublicationInfo
dgn-np:NP75852.RAvLNs9xXg7S419exdTn4AuUC-S5htGNyLR9VXlBzGwB8130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP75852.RAvLNs9xXg7S419exdTn4AuUC-S5htGNyLR9VXlBzGwB8130_assertion
a
np:Assertion
.
dgn-np:NP75852.RAvLNs9xXg7S419exdTn4AuUC-S5htGNyLR9VXlBzGwB8130_provenance
a
np:Provenance
.
dgn-np:NP75852.RAvLNs9xXg7S419exdTn4AuUC-S5htGNyLR9VXlBzGwB8130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP75852.RAvLNs9xXg7S419exdTn4AuUC-S5htGNyLR9VXlBzGwB8130_assertion
{
miriam-gene:1789
a
ncit:C16612
.
lld:C0043117
a
ncit:C7057
.
dgn-gda:DGN50ae901eb61bfe571da85165f0462fd2
sio:SIO_000628
miriam-gene:1789
,
lld:C0043117
;
a
sio:SIO_001122
.
}
dgn-np:NP75852.RAvLNs9xXg7S419exdTn4AuUC-S5htGNyLR9VXlBzGwB8130_provenance
{
dgn-np:NP75852.RAvLNs9xXg7S419exdTn4AuUC-S5htGNyLR9VXlBzGwB8130_assertion
dcterms:description
"[The purpose of this study was to investigate the association between the single nucleotide polymorphism (SNP) in promoter of the DNMT3B gene and the risk for development of idiopathic thrombocytopenic purpura (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:18437543
;
prov:wasDerivedFrom
dgn-void:gad-20130706
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:gad-20130706
pav:importedOn
"2013-07-06"^^
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:NP75852.RAvLNs9xXg7S419exdTn4AuUC-S5htGNyLR9VXlBzGwB8130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:37+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" .
}