@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP501860.RAekOsv_cQdBXj9IjyZ2Oj9muVqVqOEWZEaSijzy0CGXI
> .
@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:NP501860.RAekOsv_cQdBXj9IjyZ2Oj9muVqVqOEWZEaSijzy0CGXI130_head
{
this:
np:hasAssertion
dgn-np:NP501860.RAekOsv_cQdBXj9IjyZ2Oj9muVqVqOEWZEaSijzy0CGXI130_assertion
;
np:hasProvenance
dgn-np:NP501860.RAekOsv_cQdBXj9IjyZ2Oj9muVqVqOEWZEaSijzy0CGXI130_provenance
;
np:hasPublicationInfo
dgn-np:NP501860.RAekOsv_cQdBXj9IjyZ2Oj9muVqVqOEWZEaSijzy0CGXI130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP501860.RAekOsv_cQdBXj9IjyZ2Oj9muVqVqOEWZEaSijzy0CGXI130_assertion
a
np:Assertion
.
dgn-np:NP501860.RAekOsv_cQdBXj9IjyZ2Oj9muVqVqOEWZEaSijzy0CGXI130_provenance
a
np:Provenance
.
dgn-np:NP501860.RAekOsv_cQdBXj9IjyZ2Oj9muVqVqOEWZEaSijzy0CGXI130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP501860.RAekOsv_cQdBXj9IjyZ2Oj9muVqVqOEWZEaSijzy0CGXI130_assertion
{
miriam-gene:1814
a
ncit:C16612
.
lld:C0011581
a
ncit:C7057
.
dgn-gda:DGN476aa4998c95e418d414b88d721b7b74
sio:SIO_000628
miriam-gene:1814
,
lld:C0011581
;
a
sio:SIO_001121
.
}
dgn-np:NP501860.RAekOsv_cQdBXj9IjyZ2Oj9muVqVqOEWZEaSijzy0CGXI130_provenance
{
dgn-np:NP501860.RAekOsv_cQdBXj9IjyZ2Oj9muVqVqOEWZEaSijzy0CGXI130_assertion
dcterms:description
"[In a sample of 308 Chinese Han patients with major depressive disorder, 13 single nucleotide polymorphisms (SNPs) in coding regions of six genes (MAOA, SLC6A2, TH, COMT, DRD2, DRD3) with minor allele frequencies >5% were successfully genotyped from an initial series of 35 SNPs in 11 candidate genes associated with catecholamine neurotransmission.]. 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:21680027
;
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:NP501860.RAekOsv_cQdBXj9IjyZ2Oj9muVqVqOEWZEaSijzy0CGXI130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:59+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" .
}