@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP58784.RAE3zsx-8nIt4p35HiGkN_cgG-xd3BzGZB1GquLSRXqW0
> .
@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:NP58784.RAE3zsx-8nIt4p35HiGkN_cgG-xd3BzGZB1GquLSRXqW0130_head
{
this:
np:hasAssertion
dgn-np:NP58784.RAE3zsx-8nIt4p35HiGkN_cgG-xd3BzGZB1GquLSRXqW0130_assertion
;
np:hasProvenance
dgn-np:NP58784.RAE3zsx-8nIt4p35HiGkN_cgG-xd3BzGZB1GquLSRXqW0130_provenance
;
np:hasPublicationInfo
dgn-np:NP58784.RAE3zsx-8nIt4p35HiGkN_cgG-xd3BzGZB1GquLSRXqW0130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP58784.RAE3zsx-8nIt4p35HiGkN_cgG-xd3BzGZB1GquLSRXqW0130_assertion
a
np:Assertion
.
dgn-np:NP58784.RAE3zsx-8nIt4p35HiGkN_cgG-xd3BzGZB1GquLSRXqW0130_provenance
a
np:Provenance
.
dgn-np:NP58784.RAE3zsx-8nIt4p35HiGkN_cgG-xd3BzGZB1GquLSRXqW0130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP58784.RAE3zsx-8nIt4p35HiGkN_cgG-xd3BzGZB1GquLSRXqW0130_assertion
{
miriam-gene:7166
a
ncit:C16612
.
lld:C0001807
a
ncit:C7057
.
dgn-gda:DGN8781b557a805a7920982393be3c6a138
sio:SIO_000628
miriam-gene:7166
,
lld:C0001807
;
a
sio:SIO_001122
.
}
dgn-np:NP58784.RAE3zsx-8nIt4p35HiGkN_cgG-xd3BzGZB1GquLSRXqW0130_provenance
{
dgn-np:NP58784.RAE3zsx-8nIt4p35HiGkN_cgG-xd3BzGZB1GquLSRXqW0130_assertion
dcterms:description
"[Finally, an association study with 58 volunteers revealed that the A779C TPH polymorphism significantly relates to AH, with the highest aggression levels for the genotype AA and the lowest aggression levels for the genotype CC, but not to NH. Results are discussed with respect to inconsistent findings in the literature, which may be explained by this distinction of types of aggression.]. 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:15727508
;
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:NP58784.RAE3zsx-8nIt4p35HiGkN_cgG-xd3BzGZB1GquLSRXqW0130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:27+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" .
}