@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP383251.RAdXoMeDPsXCwfArWM9w6v8wQ8vRRYjzozO9n36KJXilg
> .
@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:NP383251.RAdXoMeDPsXCwfArWM9w6v8wQ8vRRYjzozO9n36KJXilg130_head
{
this:
np:hasAssertion
dgn-np:NP383251.RAdXoMeDPsXCwfArWM9w6v8wQ8vRRYjzozO9n36KJXilg130_assertion
;
np:hasProvenance
dgn-np:NP383251.RAdXoMeDPsXCwfArWM9w6v8wQ8vRRYjzozO9n36KJXilg130_provenance
;
np:hasPublicationInfo
dgn-np:NP383251.RAdXoMeDPsXCwfArWM9w6v8wQ8vRRYjzozO9n36KJXilg130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP383251.RAdXoMeDPsXCwfArWM9w6v8wQ8vRRYjzozO9n36KJXilg130_assertion
a
np:Assertion
.
dgn-np:NP383251.RAdXoMeDPsXCwfArWM9w6v8wQ8vRRYjzozO9n36KJXilg130_provenance
a
np:Provenance
.
dgn-np:NP383251.RAdXoMeDPsXCwfArWM9w6v8wQ8vRRYjzozO9n36KJXilg130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP383251.RAdXoMeDPsXCwfArWM9w6v8wQ8vRRYjzozO9n36KJXilg130_assertion
{
miriam-gene:775
a
ncit:C16612
.
lld:C0011570
a
ncit:C7057
.
dgn-gda:DGNe49b9b5cec88f092d20e970fa9c81c6f
sio:SIO_000628
miriam-gene:775
,
lld:C0011570
;
a
sio:SIO_001121
.
}
dgn-np:NP383251.RAdXoMeDPsXCwfArWM9w6v8wQ8vRRYjzozO9n36KJXilg130_provenance
{
dgn-np:NP383251.RAdXoMeDPsXCwfArWM9w6v8wQ8vRRYjzozO9n36KJXilg130_assertion
dcterms:description
"[Genetic variation in CACNA1C have also been associated with depression, schizophrenia, autism spectrum disorders, as well as changes in brain function and structure in control subjects who have no diagnosable psychiatric illness.]. 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:22705413
;
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:NP383251.RAdXoMeDPsXCwfArWM9w6v8wQ8vRRYjzozO9n36KJXilg130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:48+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" .
}