@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP1405941.RAhRNfKV2OY4oY7ioN0svtaHrjVxcC_tjQym2qmYLrqns
> .
@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/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@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/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v4.0.0/void/
> .
dgn-np:NP1405941.RAhRNfKV2OY4oY7ioN0svtaHrjVxcC_tjQym2qmYLrqns130_head
{
this:
np:hasAssertion
dgn-np:NP1405941.RAhRNfKV2OY4oY7ioN0svtaHrjVxcC_tjQym2qmYLrqns130_assertion
;
np:hasProvenance
dgn-np:NP1405941.RAhRNfKV2OY4oY7ioN0svtaHrjVxcC_tjQym2qmYLrqns130_provenance
;
np:hasPublicationInfo
dgn-np:NP1405941.RAhRNfKV2OY4oY7ioN0svtaHrjVxcC_tjQym2qmYLrqns130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP1405941.RAhRNfKV2OY4oY7ioN0svtaHrjVxcC_tjQym2qmYLrqns130_assertion
a
np:Assertion
.
dgn-np:NP1405941.RAhRNfKV2OY4oY7ioN0svtaHrjVxcC_tjQym2qmYLrqns130_provenance
a
np:Provenance
.
dgn-np:NP1405941.RAhRNfKV2OY4oY7ioN0svtaHrjVxcC_tjQym2qmYLrqns130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP1405941.RAhRNfKV2OY4oY7ioN0svtaHrjVxcC_tjQym2qmYLrqns130_assertion
{
miriam-gene:283120
a
ncit:C16612
.
lld:C0004903
a
ncit:C7057
.
dgn-gda:DGN5b57c986b55eb1ccaf6fa4d391404bc4
sio:SIO_000628
miriam-gene:283120
,
lld:C0004903
;
a
sio:SIO_001121
.
}
dgn-np:NP1405941.RAhRNfKV2OY4oY7ioN0svtaHrjVxcC_tjQym2qmYLrqns130_provenance
{
dgn-np:NP1405941.RAhRNfKV2OY4oY7ioN0svtaHrjVxcC_tjQym2qmYLrqns130_assertion
dcterms:description
"[We discuss these results in terms of their challenge to the prevailing dogma on the function of the enigmatic H19 gene, as well as with respect to the ontogeny of the Beckwith-Wiedemann syndrome, and propose that the human H19 gene is an antagonist of IGF2 expressivity in trans.]. 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:9774446
;
prov:wasDerivedFrom
dgn-void:befree-2016
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-2016
pav:importedOn
"2016-02-19"^^
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:NP1405941.RAhRNfKV2OY4oY7ioN0svtaHrjVxcC_tjQym2qmYLrqns130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:52:24+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:disgenetv3.0rdf
;
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
"v4.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v4.0.0" .
}