@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP314128.RApYcC79YQFOEBMaMxyn8ZhFkJf9lyAnQ058FDQJXSUJ4
> .
@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:NP314128.RApYcC79YQFOEBMaMxyn8ZhFkJf9lyAnQ058FDQJXSUJ4130_head
{
this:
np:hasAssertion
dgn-np:NP314128.RApYcC79YQFOEBMaMxyn8ZhFkJf9lyAnQ058FDQJXSUJ4130_assertion
;
np:hasProvenance
dgn-np:NP314128.RApYcC79YQFOEBMaMxyn8ZhFkJf9lyAnQ058FDQJXSUJ4130_provenance
;
np:hasPublicationInfo
dgn-np:NP314128.RApYcC79YQFOEBMaMxyn8ZhFkJf9lyAnQ058FDQJXSUJ4130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP314128.RApYcC79YQFOEBMaMxyn8ZhFkJf9lyAnQ058FDQJXSUJ4130_assertion
a
np:Assertion
.
dgn-np:NP314128.RApYcC79YQFOEBMaMxyn8ZhFkJf9lyAnQ058FDQJXSUJ4130_provenance
a
np:Provenance
.
dgn-np:NP314128.RApYcC79YQFOEBMaMxyn8ZhFkJf9lyAnQ058FDQJXSUJ4130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP314128.RApYcC79YQFOEBMaMxyn8ZhFkJf9lyAnQ058FDQJXSUJ4130_assertion
{
miriam-gene:3481
a
ncit:C16612
.
lld:C0032463
a
ncit:C7057
.
dgn-gda:DGN1cfe3dea322d0ce58c155afb2925a94f
sio:SIO_000628
miriam-gene:3481
,
lld:C0032463
;
a
sio:SIO_001121
.
}
dgn-np:NP314128.RApYcC79YQFOEBMaMxyn8ZhFkJf9lyAnQ058FDQJXSUJ4130_provenance
{
dgn-np:NP314128.RApYcC79YQFOEBMaMxyn8ZhFkJf9lyAnQ058FDQJXSUJ4130_assertion
dcterms:description
"[Taken together, these observations demonstrate that H19 and IGF2 are specifically expressed during haematopoiesis and that low levels of H19 expression are associated with PV and may contribute to the pathology of the disease.]. 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:10640993
;
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:NP314128.RApYcC79YQFOEBMaMxyn8ZhFkJf9lyAnQ058FDQJXSUJ4130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:00+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" .
}