@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP826099.RAWpJrYmTVrAqKJCRxlx3PGfUOWpNPFG5Yl9WNSa1KoeA
> .
@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:NP826099.RAWpJrYmTVrAqKJCRxlx3PGfUOWpNPFG5Yl9WNSa1KoeA130_head
{
this:
np:hasAssertion
dgn-np:NP826099.RAWpJrYmTVrAqKJCRxlx3PGfUOWpNPFG5Yl9WNSa1KoeA130_assertion
;
np:hasProvenance
dgn-np:NP826099.RAWpJrYmTVrAqKJCRxlx3PGfUOWpNPFG5Yl9WNSa1KoeA130_provenance
;
np:hasPublicationInfo
dgn-np:NP826099.RAWpJrYmTVrAqKJCRxlx3PGfUOWpNPFG5Yl9WNSa1KoeA130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP826099.RAWpJrYmTVrAqKJCRxlx3PGfUOWpNPFG5Yl9WNSa1KoeA130_assertion
a
np:Assertion
.
dgn-np:NP826099.RAWpJrYmTVrAqKJCRxlx3PGfUOWpNPFG5Yl9WNSa1KoeA130_provenance
a
np:Provenance
.
dgn-np:NP826099.RAWpJrYmTVrAqKJCRxlx3PGfUOWpNPFG5Yl9WNSa1KoeA130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP826099.RAWpJrYmTVrAqKJCRxlx3PGfUOWpNPFG5Yl9WNSa1KoeA130_assertion
{
miriam-gene:3342
a
ncit:C16612
.
lld:C0010314
a
ncit:C7057
.
dgn-gda:DGNb440a0d35f22fdc212b5a013655e6c0e
sio:SIO_000628
miriam-gene:3342
,
lld:C0010314
;
a
sio:SIO_001121
.
}
dgn-np:NP826099.RAWpJrYmTVrAqKJCRxlx3PGfUOWpNPFG5Yl9WNSa1KoeA130_provenance
{
dgn-np:NP826099.RAWpJrYmTVrAqKJCRxlx3PGfUOWpNPFG5Yl9WNSa1KoeA130_assertion
dcterms:description
"[The combination of FISH, CGH, and cytogenetics has confirmed that the characteristic cry of the cri du chat syndrome is due to the deletion of the most distal part of the classic del 5p region.]. 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:11891684
;
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:NP826099.RAWpJrYmTVrAqKJCRxlx3PGfUOWpNPFG5Yl9WNSa1KoeA130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:25+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" .
}