@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP54978.RAiQgrJ0ud30Hk1UkF_ISCGwZCJHgdZhDmBmqaARV1ONg
> .
@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:NP54978.RAiQgrJ0ud30Hk1UkF_ISCGwZCJHgdZhDmBmqaARV1ONg130_head
{
this:
np:hasAssertion
dgn-np:NP54978.RAiQgrJ0ud30Hk1UkF_ISCGwZCJHgdZhDmBmqaARV1ONg130_assertion
;
np:hasProvenance
dgn-np:NP54978.RAiQgrJ0ud30Hk1UkF_ISCGwZCJHgdZhDmBmqaARV1ONg130_provenance
;
np:hasPublicationInfo
dgn-np:NP54978.RAiQgrJ0ud30Hk1UkF_ISCGwZCJHgdZhDmBmqaARV1ONg130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP54978.RAiQgrJ0ud30Hk1UkF_ISCGwZCJHgdZhDmBmqaARV1ONg130_assertion
a
np:Assertion
.
dgn-np:NP54978.RAiQgrJ0ud30Hk1UkF_ISCGwZCJHgdZhDmBmqaARV1ONg130_provenance
a
np:Provenance
.
dgn-np:NP54978.RAiQgrJ0ud30Hk1UkF_ISCGwZCJHgdZhDmBmqaARV1ONg130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP54978.RAiQgrJ0ud30Hk1UkF_ISCGwZCJHgdZhDmBmqaARV1ONg130_assertion
{
miriam-gene:4128
a
ncit:C16612
.
lld:C1842981
a
ncit:C7057
.
dgn-gda:DGN9f84f8391818d95192837f816365a077
sio:SIO_000628
miriam-gene:4128
,
lld:C1842981
;
a
sio:SIO_001122
.
}
dgn-np:NP54978.RAiQgrJ0ud30Hk1UkF_ISCGwZCJHgdZhDmBmqaARV1ONg130_provenance
{
dgn-np:NP54978.RAiQgrJ0ud30Hk1UkF_ISCGwZCJHgdZhDmBmqaARV1ONg130_assertion
dcterms:description
"[We found weak evidence for association with COMT genotype, when the females and males were considered separately, and for MAOA genotype in males only. There was no significant interaction between COMT and MAOA.]. 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:12815746
;
prov:wasDerivedFrom
dgn-void:gad-20130706
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:gad-20130706
pav:importedOn
"2013-07-06"^^
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:NP54978.RAiQgrJ0ud30Hk1UkF_ISCGwZCJHgdZhDmBmqaARV1ONg130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:25+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" .
}