@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP802806.RAYYSkBxq71KpN6QDAz5tVAaBHpvwH2dzrP6ZJIhz_N_s
> .
@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:NP802806.RAYYSkBxq71KpN6QDAz5tVAaBHpvwH2dzrP6ZJIhz_N_s130_head
{
this:
np:hasAssertion
dgn-np:NP802806.RAYYSkBxq71KpN6QDAz5tVAaBHpvwH2dzrP6ZJIhz_N_s130_assertion
;
np:hasProvenance
dgn-np:NP802806.RAYYSkBxq71KpN6QDAz5tVAaBHpvwH2dzrP6ZJIhz_N_s130_provenance
;
np:hasPublicationInfo
dgn-np:NP802806.RAYYSkBxq71KpN6QDAz5tVAaBHpvwH2dzrP6ZJIhz_N_s130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP802806.RAYYSkBxq71KpN6QDAz5tVAaBHpvwH2dzrP6ZJIhz_N_s130_assertion
a
np:Assertion
.
dgn-np:NP802806.RAYYSkBxq71KpN6QDAz5tVAaBHpvwH2dzrP6ZJIhz_N_s130_provenance
a
np:Provenance
.
dgn-np:NP802806.RAYYSkBxq71KpN6QDAz5tVAaBHpvwH2dzrP6ZJIhz_N_s130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP802806.RAYYSkBxq71KpN6QDAz5tVAaBHpvwH2dzrP6ZJIhz_N_s130_assertion
{
miriam-gene:4129
a
ncit:C16612
.
lld:C0525045
a
ncit:C7057
.
dgn-gda:DGN8d35ce5063a93c5cc74271bca1d17d66
sio:SIO_000628
miriam-gene:4129
,
lld:C0525045
;
a
sio:SIO_001121
.
}
dgn-np:NP802806.RAYYSkBxq71KpN6QDAz5tVAaBHpvwH2dzrP6ZJIhz_N_s130_provenance
{
dgn-np:NP802806.RAYYSkBxq71KpN6QDAz5tVAaBHpvwH2dzrP6ZJIhz_N_s130_assertion
dcterms:description
"[To ascertain whether mood disorders, including bipolar and unipolar, are genetically associated with the monoamine oxidase A (MAOA) or monoamine oxidase B (MAOB) gene in the Chinese population, 132 cases of mood disorder and 88 normal controls were genotyped for the MAOA(CA)n, MAOB(GT)n, and MAOB(TG)n loci by the method of amplification fragment length polymorphism.]. 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:10686545
;
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:NP802806.RAYYSkBxq71KpN6QDAz5tVAaBHpvwH2dzrP6ZJIhz_N_s130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:12+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" .
}