@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP880899.RA4LblnAqagooeFUhxuAlSzvbzv_2YDS-WDWvJz4KfV3E
> .
@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#
> .
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{
this:
np:hasAssertion
dgn-np:NP880899.RA4LblnAqagooeFUhxuAlSzvbzv_2YDS-WDWvJz4KfV3E130_assertion
;
np:hasProvenance
dgn-np:NP880899.RA4LblnAqagooeFUhxuAlSzvbzv_2YDS-WDWvJz4KfV3E130_provenance
;
np:hasPublicationInfo
dgn-np:NP880899.RA4LblnAqagooeFUhxuAlSzvbzv_2YDS-WDWvJz4KfV3E130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP880899.RA4LblnAqagooeFUhxuAlSzvbzv_2YDS-WDWvJz4KfV3E130_assertion
a
np:Assertion
.
dgn-np:NP880899.RA4LblnAqagooeFUhxuAlSzvbzv_2YDS-WDWvJz4KfV3E130_provenance
a
np:Provenance
.
dgn-np:NP880899.RA4LblnAqagooeFUhxuAlSzvbzv_2YDS-WDWvJz4KfV3E130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP880899.RA4LblnAqagooeFUhxuAlSzvbzv_2YDS-WDWvJz4KfV3E130_assertion
{
miriam-gene:91752
a
ncit:C16612
.
lld:C0525045
a
ncit:C7057
.
dgn-gda:DGN5db4b84caa70e51d082c91b9d1dfa5fc
sio:SIO_000628
miriam-gene:91752
,
lld:C0525045
;
a
sio:SIO_001121
.
}
dgn-np:NP880899.RA4LblnAqagooeFUhxuAlSzvbzv_2YDS-WDWvJz4KfV3E130_provenance
{
dgn-np:NP880899.RA4LblnAqagooeFUhxuAlSzvbzv_2YDS-WDWvJz4KfV3E130_assertion
dcterms:description
"[We therefore wanted to examine whether the reported BD genetic variants in CACNA1C, ANK3, MYO5B, TSPAN8 and ZNF804A loci are associated with ADHD or with scores on the Mood Disorder Questionnaire (MDQ), a commonly used screening instrument for bipolar spectrum disorders.]. 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:21276201
;
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:NP880899.RA4LblnAqagooeFUhxuAlSzvbzv_2YDS-WDWvJz4KfV3E130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:58+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" .
}