@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP95391.RAC4cjAyhJqSWqDRqcAl28G8YjjHv82SQpNeL893yiknw
> .
@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:NP95391.RAC4cjAyhJqSWqDRqcAl28G8YjjHv82SQpNeL893yiknw130_head
{
this:
np:hasAssertion
dgn-np:NP95391.RAC4cjAyhJqSWqDRqcAl28G8YjjHv82SQpNeL893yiknw130_assertion
;
np:hasProvenance
dgn-np:NP95391.RAC4cjAyhJqSWqDRqcAl28G8YjjHv82SQpNeL893yiknw130_provenance
;
np:hasPublicationInfo
dgn-np:NP95391.RAC4cjAyhJqSWqDRqcAl28G8YjjHv82SQpNeL893yiknw130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP95391.RAC4cjAyhJqSWqDRqcAl28G8YjjHv82SQpNeL893yiknw130_assertion
a
np:Assertion
.
dgn-np:NP95391.RAC4cjAyhJqSWqDRqcAl28G8YjjHv82SQpNeL893yiknw130_provenance
a
np:Provenance
.
dgn-np:NP95391.RAC4cjAyhJqSWqDRqcAl28G8YjjHv82SQpNeL893yiknw130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP95391.RAC4cjAyhJqSWqDRqcAl28G8YjjHv82SQpNeL893yiknw130_assertion
{
miriam-gene:84700
a
ncit:C16612
.
lld:C0004936
a
ncit:C7057
.
dgn-gda:DGNb9d3a115f000b879e0c455d762dc0496
sio:SIO_000628
miriam-gene:84700
,
lld:C0004936
;
a
sio:SIO_001122
.
}
dgn-np:NP95391.RAC4cjAyhJqSWqDRqcAl28G8YjjHv82SQpNeL893yiknw130_provenance
{
dgn-np:NP95391.RAC4cjAyhJqSWqDRqcAl28G8YjjHv82SQpNeL893yiknw130_assertion
dcterms:description
"[This study provides the first genomewide significant evidence implicating variants near the ADM gene on chromosome 11p15 in psychopathology, with effects that appear to be specific to bipolar II disorder. Although genomewide significant evidence of cross-disorder effects was not detected, the results provide evidence that there are both pleiotropic and disorder-specific effects on major mental illness and illustrate an approach to dissecting the genetic basis of mood and psychotic disorders that can inform future large-scale cross-disorder GWAS analyses.]. 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:20713499
;
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:NP95391.RAC4cjAyhJqSWqDRqcAl28G8YjjHv82SQpNeL893yiknw130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:47+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" .
}