@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP665377.RA_S1H4lSCGtnZbtBfNRRIeDQpRkU7Fi9MdCUpCsCXx48
> .
@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:NP665377.RA_S1H4lSCGtnZbtBfNRRIeDQpRkU7Fi9MdCUpCsCXx48130_head
{
this:
np:hasAssertion
dgn-np:NP665377.RA_S1H4lSCGtnZbtBfNRRIeDQpRkU7Fi9MdCUpCsCXx48130_assertion
;
np:hasProvenance
dgn-np:NP665377.RA_S1H4lSCGtnZbtBfNRRIeDQpRkU7Fi9MdCUpCsCXx48130_provenance
;
np:hasPublicationInfo
dgn-np:NP665377.RA_S1H4lSCGtnZbtBfNRRIeDQpRkU7Fi9MdCUpCsCXx48130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP665377.RA_S1H4lSCGtnZbtBfNRRIeDQpRkU7Fi9MdCUpCsCXx48130_assertion
a
np:Assertion
.
dgn-np:NP665377.RA_S1H4lSCGtnZbtBfNRRIeDQpRkU7Fi9MdCUpCsCXx48130_provenance
a
np:Provenance
.
dgn-np:NP665377.RA_S1H4lSCGtnZbtBfNRRIeDQpRkU7Fi9MdCUpCsCXx48130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP665377.RA_S1H4lSCGtnZbtBfNRRIeDQpRkU7Fi9MdCUpCsCXx48130_assertion
{
miriam-gene:1312
a
ncit:C16612
.
lld:C0424101
a
ncit:C7057
.
dgn-gda:DGN4cad947bee7a8de756d55c2066039c22
sio:SIO_000628
miriam-gene:1312
,
lld:C0424101
;
a
sio:SIO_001121
.
}
dgn-np:NP665377.RA_S1H4lSCGtnZbtBfNRRIeDQpRkU7Fi9MdCUpCsCXx48130_provenance
{
dgn-np:NP665377.RA_S1H4lSCGtnZbtBfNRRIeDQpRkU7Fi9MdCUpCsCXx48130_assertion
dcterms:description
"[We previously reported an association in 48 ADHD triads (both parents and proband) between the catechol-O-methyl- transferase (COMT) polymorphism (especially the high enzyme activity val allele) and the Diagnostic and Statistical Manual of Mental Disorders (DSM IV) combined category (excluding inattention) of ADHD (however, see erratum, Am.]. 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:11121197
;
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:NP665377.RA_S1H4lSCGtnZbtBfNRRIeDQpRkU7Fi9MdCUpCsCXx48130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:42+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" .
}