@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP265066.RAYW7c7hjCRFL9kI4YuKEeyItzcWl_qfN67_uox4Alj2g
> .
@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#
> .
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{
this:
np:hasAssertion
dgn-np:NP265066.RAYW7c7hjCRFL9kI4YuKEeyItzcWl_qfN67_uox4Alj2g130_assertion
;
np:hasProvenance
dgn-np:NP265066.RAYW7c7hjCRFL9kI4YuKEeyItzcWl_qfN67_uox4Alj2g130_provenance
;
np:hasPublicationInfo
dgn-np:NP265066.RAYW7c7hjCRFL9kI4YuKEeyItzcWl_qfN67_uox4Alj2g130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP265066.RAYW7c7hjCRFL9kI4YuKEeyItzcWl_qfN67_uox4Alj2g130_assertion
a
np:Assertion
.
dgn-np:NP265066.RAYW7c7hjCRFL9kI4YuKEeyItzcWl_qfN67_uox4Alj2g130_provenance
a
np:Provenance
.
dgn-np:NP265066.RAYW7c7hjCRFL9kI4YuKEeyItzcWl_qfN67_uox4Alj2g130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP265066.RAYW7c7hjCRFL9kI4YuKEeyItzcWl_qfN67_uox4Alj2g130_assertion
{
miriam-gene:181
a
ncit:C16612
.
lld:C0004903
a
ncit:C7057
.
dgn-gda:DGN9c4867b3b341455fa124748ee0b53151
sio:SIO_000628
miriam-gene:181
,
lld:C0004903
;
a
sio:SIO_001121
.
}
dgn-np:NP265066.RAYW7c7hjCRFL9kI4YuKEeyItzcWl_qfN67_uox4Alj2g130_provenance
{
dgn-np:NP265066.RAYW7c7hjCRFL9kI4YuKEeyItzcWl_qfN67_uox4Alj2g130_assertion
dcterms:description
"[In this review, we describe the latest knowledge surrounding the imprinting mechanism of 11p15.5, in addition to epigenetic and genetic etiologies of BWS, associated childhood tumors, the effects of ART and multilocus hypomethylation disorders.]. 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:23719190
;
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:NP265066.RAYW7c7hjCRFL9kI4YuKEeyItzcWl_qfN67_uox4Alj2g130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:28+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
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"v2.1.0" .
}