@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP767214.RA_VSgtB0MtSYkJMC8ZTr7Lote3A7kFWiGoeKtrCDZwIs
> .
@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:NP767214.RA_VSgtB0MtSYkJMC8ZTr7Lote3A7kFWiGoeKtrCDZwIs130_head
{
this:
np:hasAssertion
dgn-np:NP767214.RA_VSgtB0MtSYkJMC8ZTr7Lote3A7kFWiGoeKtrCDZwIs130_assertion
;
np:hasProvenance
dgn-np:NP767214.RA_VSgtB0MtSYkJMC8ZTr7Lote3A7kFWiGoeKtrCDZwIs130_provenance
;
np:hasPublicationInfo
dgn-np:NP767214.RA_VSgtB0MtSYkJMC8ZTr7Lote3A7kFWiGoeKtrCDZwIs130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP767214.RA_VSgtB0MtSYkJMC8ZTr7Lote3A7kFWiGoeKtrCDZwIs130_assertion
a
np:Assertion
.
dgn-np:NP767214.RA_VSgtB0MtSYkJMC8ZTr7Lote3A7kFWiGoeKtrCDZwIs130_provenance
a
np:Provenance
.
dgn-np:NP767214.RA_VSgtB0MtSYkJMC8ZTr7Lote3A7kFWiGoeKtrCDZwIs130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP767214.RA_VSgtB0MtSYkJMC8ZTr7Lote3A7kFWiGoeKtrCDZwIs130_assertion
{
miriam-gene:7389
a
ncit:C16612
.
lld:C0032897
a
ncit:C7057
.
dgn-gda:DGN0ed00858098d0b05b9b27c4a980cc9fe
sio:SIO_000628
miriam-gene:7389
,
lld:C0032897
;
a
sio:SIO_001121
.
}
dgn-np:NP767214.RA_VSgtB0MtSYkJMC8ZTr7Lote3A7kFWiGoeKtrCDZwIs130_provenance
{
dgn-np:NP767214.RA_VSgtB0MtSYkJMC8ZTr7Lote3A7kFWiGoeKtrCDZwIs130_assertion
dcterms:description
"[Nine probands with a firm clinical diagnosis of PWS but who had neither a typical deletion in the PWS region nor UPD(15)mat were investigated for inactivating mutations in 11 genes located in the PWS region, including SNURF and SNRPN, which are associated with the imprinting centre.]. 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:17262171
;
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:NP767214.RA_VSgtB0MtSYkJMC8ZTr7Lote3A7kFWiGoeKtrCDZwIs130_publicationInfo
{
this:
dcterms:created
"2015-08-25T14:45:23+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" .
}