@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP586706.RAv16iEFV3DBhhhX9kG93yeu0i2BEcH0198LJNbMcrt-0
> .
@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:NP586706.RAv16iEFV3DBhhhX9kG93yeu0i2BEcH0198LJNbMcrt-0130_head
{
this:
np:hasAssertion
dgn-np:NP586706.RAv16iEFV3DBhhhX9kG93yeu0i2BEcH0198LJNbMcrt-0130_assertion
;
np:hasProvenance
dgn-np:NP586706.RAv16iEFV3DBhhhX9kG93yeu0i2BEcH0198LJNbMcrt-0130_provenance
;
np:hasPublicationInfo
dgn-np:NP586706.RAv16iEFV3DBhhhX9kG93yeu0i2BEcH0198LJNbMcrt-0130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP586706.RAv16iEFV3DBhhhX9kG93yeu0i2BEcH0198LJNbMcrt-0130_assertion
a
np:Assertion
.
dgn-np:NP586706.RAv16iEFV3DBhhhX9kG93yeu0i2BEcH0198LJNbMcrt-0130_provenance
a
np:Provenance
.
dgn-np:NP586706.RAv16iEFV3DBhhhX9kG93yeu0i2BEcH0198LJNbMcrt-0130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP586706.RAv16iEFV3DBhhhX9kG93yeu0i2BEcH0198LJNbMcrt-0130_assertion
{
miriam-gene:2562
a
ncit:C16612
.
lld:C0162635
a
ncit:C7057
.
dgn-gda:DGN5e2613aee79e193c978246176e91e97d
sio:SIO_000628
miriam-gene:2562
,
lld:C0162635
;
a
sio:SIO_001121
.
}
dgn-np:NP586706.RAv16iEFV3DBhhhX9kG93yeu0i2BEcH0198LJNbMcrt-0130_provenance
{
dgn-np:NP586706.RAv16iEFV3DBhhhX9kG93yeu0i2BEcH0198LJNbMcrt-0130_assertion
dcterms:description
"[In a series of 18 individuals comprising parents of Angelman syndrome (AS) patients and AS patients with large deletions, microdeletions, and no deletions, we utilized fluorescence in situ hybridization (FISH) with genomic phage clones for loci D15S63 and GABRB3 for deletion detection of chromosome 15q11-q13.]. 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:7747771
;
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:NP586706.RAv16iEFV3DBhhhX9kG93yeu0i2BEcH0198LJNbMcrt-0130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:53+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" .
}