@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP764983.RANv0MVyBR86B57ejGfBWZ60D_dRvyKCQJ4HcapbF36Lc
> .
@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/v3.0.0/void/
> .
dgn-np:NP764983.RANv0MVyBR86B57ejGfBWZ60D_dRvyKCQJ4HcapbF36Lc130_head
{
this:
np:hasAssertion
dgn-np:NP764983.RANv0MVyBR86B57ejGfBWZ60D_dRvyKCQJ4HcapbF36Lc130_assertion
;
np:hasProvenance
dgn-np:NP764983.RANv0MVyBR86B57ejGfBWZ60D_dRvyKCQJ4HcapbF36Lc130_provenance
;
np:hasPublicationInfo
dgn-np:NP764983.RANv0MVyBR86B57ejGfBWZ60D_dRvyKCQJ4HcapbF36Lc130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP764983.RANv0MVyBR86B57ejGfBWZ60D_dRvyKCQJ4HcapbF36Lc130_assertion
a
np:Assertion
.
dgn-np:NP764983.RANv0MVyBR86B57ejGfBWZ60D_dRvyKCQJ4HcapbF36Lc130_provenance
a
np:Provenance
.
dgn-np:NP764983.RANv0MVyBR86B57ejGfBWZ60D_dRvyKCQJ4HcapbF36Lc130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP764983.RANv0MVyBR86B57ejGfBWZ60D_dRvyKCQJ4HcapbF36Lc130_assertion
{
miriam-gene:7337
a
ncit:C16612
.
lld:C0032897
a
ncit:C7057
.
dgn-gda:DGN719f8f0583d5dc00527c059d74b33210
sio:SIO_000628
miriam-gene:7337
,
lld:C0032897
;
a
sio:SIO_001121
.
}
dgn-np:NP764983.RANv0MVyBR86B57ejGfBWZ60D_dRvyKCQJ4HcapbF36Lc130_provenance
{
dgn-np:NP764983.RANv0MVyBR86B57ejGfBWZ60D_dRvyKCQJ4HcapbF36Lc130_assertion
dcterms:description
"[These iPSC models of genomic imprinting disorders will facilitate investigation of the AS and PWS disease processes and allow study of the developmental timing and mechanism of UBE3A repression in human neurons.]. 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:20876107
;
prov:wasDerivedFrom
dgn-void:befree-20150227
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-20150227
pav:importedOn
"2015-02-27"^^
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:NP764983.RANv0MVyBR86B57ejGfBWZ60D_dRvyKCQJ4HcapbF36Lc130_publicationInfo
{
this:
dcterms:created
"2015-08-25T14:45:22+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
"v3.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v3.0.0" .
}