@prefix dc: <
http://purl.org/dc/terms/
> .
@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP379886.RAD70VAydnr54ZdpSSN7qM6XJWl2r8YlYiztJK43vcFiI
> .
@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 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:NP379886.RAD70VAydnr54ZdpSSN7qM6XJWl2r8YlYiztJK43vcFiI130_head
{
this:
np:hasAssertion
dgn-np:NP379886.RAD70VAydnr54ZdpSSN7qM6XJWl2r8YlYiztJK43vcFiI130_assertion
;
np:hasProvenance
dgn-np:NP379886.RAD70VAydnr54ZdpSSN7qM6XJWl2r8YlYiztJK43vcFiI130_provenance
;
np:hasPublicationInfo
dgn-np:NP379886.RAD70VAydnr54ZdpSSN7qM6XJWl2r8YlYiztJK43vcFiI130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP379886.RAD70VAydnr54ZdpSSN7qM6XJWl2r8YlYiztJK43vcFiI130_assertion
a
np:Assertion
.
dgn-np:NP379886.RAD70VAydnr54ZdpSSN7qM6XJWl2r8YlYiztJK43vcFiI130_provenance
a
np:Provenance
.
dgn-np:NP379886.RAD70VAydnr54ZdpSSN7qM6XJWl2r8YlYiztJK43vcFiI130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP379886.RAD70VAydnr54ZdpSSN7qM6XJWl2r8YlYiztJK43vcFiI130_assertion
{
miriam-gene:23230
a
ncit:C16612
.
lld:C0393576
a
ncit:C7057
.
dgn-gda:DGNa89bccc176c1f238c34fc2e443a8de85
sio:SIO_000628
miriam-gene:23230
,
lld:C0393576
;
a
sio:SIO_001121
.
}
dgn-np:NP379886.RAD70VAydnr54ZdpSSN7qM6XJWl2r8YlYiztJK43vcFiI130_provenance
{
dgn-np:NP379886.RAD70VAydnr54ZdpSSN7qM6XJWl2r8YlYiztJK43vcFiI130_assertion
dc:description
"[We performed a comprehensive mutation screen of VPS13A and XK, the gene responsible for ChAc and MLS, respectively, in 85 mood disorder subjects and XK in 86 schizophrenia subjects and compared the variants to 100 or more control alleles.]. 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:21145924
;
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:NP379886.RAD70VAydnr54ZdpSSN7qM6XJWl2r8YlYiztJK43vcFiI130_publicationInfo
{
this:
dc:created
"2014-10-02T12:35:44+02:00"^^
xsd:dateTime
;
dc:rights
<
http://opendatacommons.org/licenses/odbl/1.0/
> ;
dc:rightsHolder
dgn-void:IBIGroup
;
dc: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" .
}