@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP600212.RAGnXciX7sOPFBIGyg0emMm0Crz6UyhWtd0_-9wJGo108
> .
@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:NP600212.RAGnXciX7sOPFBIGyg0emMm0Crz6UyhWtd0_-9wJGo108130_head
{
this:
np:hasAssertion
dgn-np:NP600212.RAGnXciX7sOPFBIGyg0emMm0Crz6UyhWtd0_-9wJGo108130_assertion
;
np:hasProvenance
dgn-np:NP600212.RAGnXciX7sOPFBIGyg0emMm0Crz6UyhWtd0_-9wJGo108130_provenance
;
np:hasPublicationInfo
dgn-np:NP600212.RAGnXciX7sOPFBIGyg0emMm0Crz6UyhWtd0_-9wJGo108130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP600212.RAGnXciX7sOPFBIGyg0emMm0Crz6UyhWtd0_-9wJGo108130_assertion
a
np:Assertion
.
dgn-np:NP600212.RAGnXciX7sOPFBIGyg0emMm0Crz6UyhWtd0_-9wJGo108130_provenance
a
np:Provenance
.
dgn-np:NP600212.RAGnXciX7sOPFBIGyg0emMm0Crz6UyhWtd0_-9wJGo108130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP600212.RAGnXciX7sOPFBIGyg0emMm0Crz6UyhWtd0_-9wJGo108130_assertion
{
miriam-gene:79740
a
ncit:C16612
.
lld:C1263846
a
ncit:C7057
.
dgn-gda:DGN1dda1da1e0380d1d28804c4acc4090c9
sio:SIO_000628
miriam-gene:79740
,
lld:C1263846
;
a
sio:SIO_001121
.
}
dgn-np:NP600212.RAGnXciX7sOPFBIGyg0emMm0Crz6UyhWtd0_-9wJGo108130_provenance
{
dgn-np:NP600212.RAGnXciX7sOPFBIGyg0emMm0Crz6UyhWtd0_-9wJGo108130_assertion
dcterms:description
"[We also detected rare inherited CNVs in 19 of 248 (7.7%) ADHD probands, which were absent in 2357 controls and which either overlapped previously implicated ADHD loci (for example, DRD5 and 15q13 microduplication) or identified new candidate susceptibility genes (ASTN2, CPLX2, ZBBX, and PTPRN2).]. 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:21832240
;
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:NP600212.RAGnXciX7sOPFBIGyg0emMm0Crz6UyhWtd0_-9wJGo108130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:00+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" .
}