@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP492852.RAZFPNxmBL9AkZ4BcM9a9eVnjlkBDaAaKSUyvOk0kTt-c
> .
@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:NP492852.RAZFPNxmBL9AkZ4BcM9a9eVnjlkBDaAaKSUyvOk0kTt-c130_head
{
this:
np:hasAssertion
dgn-np:NP492852.RAZFPNxmBL9AkZ4BcM9a9eVnjlkBDaAaKSUyvOk0kTt-c130_assertion
;
np:hasProvenance
dgn-np:NP492852.RAZFPNxmBL9AkZ4BcM9a9eVnjlkBDaAaKSUyvOk0kTt-c130_provenance
;
np:hasPublicationInfo
dgn-np:NP492852.RAZFPNxmBL9AkZ4BcM9a9eVnjlkBDaAaKSUyvOk0kTt-c130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP492852.RAZFPNxmBL9AkZ4BcM9a9eVnjlkBDaAaKSUyvOk0kTt-c130_assertion
a
np:Assertion
.
dgn-np:NP492852.RAZFPNxmBL9AkZ4BcM9a9eVnjlkBDaAaKSUyvOk0kTt-c130_provenance
a
np:Provenance
.
dgn-np:NP492852.RAZFPNxmBL9AkZ4BcM9a9eVnjlkBDaAaKSUyvOk0kTt-c130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP492852.RAZFPNxmBL9AkZ4BcM9a9eVnjlkBDaAaKSUyvOk0kTt-c130_assertion
{
miriam-gene:6532
a
ncit:C16612
.
lld:C0003431
a
ncit:C7057
.
dgn-gda:DGN0bafb9e2f94f3769437987b6c68136eb
sio:SIO_000628
miriam-gene:6532
,
lld:C0003431
;
a
sio:SIO_001121
.
}
dgn-np:NP492852.RAZFPNxmBL9AkZ4BcM9a9eVnjlkBDaAaKSUyvOk0kTt-c130_provenance
{
dgn-np:NP492852.RAZFPNxmBL9AkZ4BcM9a9eVnjlkBDaAaKSUyvOk0kTt-c130_assertion
dcterms:description
"[Monoamine oxidase (MAOA) and the serotonin transporter (5HTT) are reviewed at length, as these genes have received significant scientific attention in recent years and are sites of high biological plausibility in antisocial spectrum disorders and psychopathy.]. 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:20422643
;
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:NP492852.RAZFPNxmBL9AkZ4BcM9a9eVnjlkBDaAaKSUyvOk0kTt-c130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:54+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" .
}