@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP538809.RAd2gCBcbG9XRQO90OaJ2MXXTC6Lqr1ABdtQlGCbYBYHE
> .
@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:NP538809.RAd2gCBcbG9XRQO90OaJ2MXXTC6Lqr1ABdtQlGCbYBYHE130_head
{
this:
np:hasAssertion
dgn-np:NP538809.RAd2gCBcbG9XRQO90OaJ2MXXTC6Lqr1ABdtQlGCbYBYHE130_assertion
;
np:hasProvenance
dgn-np:NP538809.RAd2gCBcbG9XRQO90OaJ2MXXTC6Lqr1ABdtQlGCbYBYHE130_provenance
;
np:hasPublicationInfo
dgn-np:NP538809.RAd2gCBcbG9XRQO90OaJ2MXXTC6Lqr1ABdtQlGCbYBYHE130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP538809.RAd2gCBcbG9XRQO90OaJ2MXXTC6Lqr1ABdtQlGCbYBYHE130_assertion
a
np:Assertion
.
dgn-np:NP538809.RAd2gCBcbG9XRQO90OaJ2MXXTC6Lqr1ABdtQlGCbYBYHE130_provenance
a
np:Provenance
.
dgn-np:NP538809.RAd2gCBcbG9XRQO90OaJ2MXXTC6Lqr1ABdtQlGCbYBYHE130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP538809.RAd2gCBcbG9XRQO90OaJ2MXXTC6Lqr1ABdtQlGCbYBYHE130_assertion
{
miriam-gene:79947
a
ncit:C16612
.
lld:C1263846
a
ncit:C7057
.
dgn-gda:DGN9475a0ddfd9c0321890c5e7866d51186
sio:SIO_000628
miriam-gene:79947
,
lld:C1263846
;
a
sio:SIO_001121
.
}
dgn-np:NP538809.RAd2gCBcbG9XRQO90OaJ2MXXTC6Lqr1ABdtQlGCbYBYHE130_provenance
{
dgn-np:NP538809.RAd2gCBcbG9XRQO90OaJ2MXXTC6Lqr1ABdtQlGCbYBYHE130_assertion
dcterms:description
"[The use of the Continuous Performance Test (CPT), as an endophenotypic measure, is valuable for genetic studies because it may show increased sensitivity to specific dimensions in attention deficit hyperactivity disorder.]. 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:14584093
;
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:NP538809.RAd2gCBcbG9XRQO90OaJ2MXXTC6Lqr1ABdtQlGCbYBYHE130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:25+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" .
}