@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP165137.RA4aXDs0UUY592exjuvvil6iuJVkZcfjlyUVKiTpMDKb8
> .
@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:NP165137.RA4aXDs0UUY592exjuvvil6iuJVkZcfjlyUVKiTpMDKb8130_head
{
this:
np:hasAssertion
dgn-np:NP165137.RA4aXDs0UUY592exjuvvil6iuJVkZcfjlyUVKiTpMDKb8130_assertion
;
np:hasProvenance
dgn-np:NP165137.RA4aXDs0UUY592exjuvvil6iuJVkZcfjlyUVKiTpMDKb8130_provenance
;
np:hasPublicationInfo
dgn-np:NP165137.RA4aXDs0UUY592exjuvvil6iuJVkZcfjlyUVKiTpMDKb8130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP165137.RA4aXDs0UUY592exjuvvil6iuJVkZcfjlyUVKiTpMDKb8130_assertion
a
np:Assertion
.
dgn-np:NP165137.RA4aXDs0UUY592exjuvvil6iuJVkZcfjlyUVKiTpMDKb8130_provenance
a
np:Provenance
.
dgn-np:NP165137.RA4aXDs0UUY592exjuvvil6iuJVkZcfjlyUVKiTpMDKb8130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP165137.RA4aXDs0UUY592exjuvvil6iuJVkZcfjlyUVKiTpMDKb8130_assertion
{
miriam-gene:1028
a
ncit:C16612
.
lld:C0004903
a
ncit:C7057
.
dgn-gda:DGNd34f0b9fd34896dd31bbf759ed2439ff
sio:SIO_000628
miriam-gene:1028
,
lld:C0004903
;
a
sio:SIO_001121
.
}
dgn-np:NP165137.RA4aXDs0UUY592exjuvvil6iuJVkZcfjlyUVKiTpMDKb8130_provenance
{
dgn-np:NP165137.RA4aXDs0UUY592exjuvvil6iuJVkZcfjlyUVKiTpMDKb8130_assertion
dcterms:description
"[The low frequency of p57KIP2 mutations, as well as our recent discovery of disruption of the K(v)LQT1 gene in patients with chromosomal rearrangements, suggest that BWS can involve disruption of multiple independent 11p15.5 genes.]. 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:9311734
;
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:NP165137.RA4aXDs0UUY592exjuvvil6iuJVkZcfjlyUVKiTpMDKb8130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:29+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" .
}