@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP730481.RA7ecRrl1grL78LYAg2019S0Ht14TVnox2pKYPZNGEzFA
> .
@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/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@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/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v4.0.0/void/
> .
dgn-np:NP730481.RA7ecRrl1grL78LYAg2019S0Ht14TVnox2pKYPZNGEzFA130_head
{
this:
np:hasAssertion
dgn-np:NP730481.RA7ecRrl1grL78LYAg2019S0Ht14TVnox2pKYPZNGEzFA130_assertion
;
np:hasProvenance
dgn-np:NP730481.RA7ecRrl1grL78LYAg2019S0Ht14TVnox2pKYPZNGEzFA130_provenance
;
np:hasPublicationInfo
dgn-np:NP730481.RA7ecRrl1grL78LYAg2019S0Ht14TVnox2pKYPZNGEzFA130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP730481.RA7ecRrl1grL78LYAg2019S0Ht14TVnox2pKYPZNGEzFA130_assertion
a
np:Assertion
.
dgn-np:NP730481.RA7ecRrl1grL78LYAg2019S0Ht14TVnox2pKYPZNGEzFA130_provenance
a
np:Provenance
.
dgn-np:NP730481.RA7ecRrl1grL78LYAg2019S0Ht14TVnox2pKYPZNGEzFA130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP730481.RA7ecRrl1grL78LYAg2019S0Ht14TVnox2pKYPZNGEzFA130_assertion
{
miriam-gene:9378
a
ncit:C16612
.
lld:C0036341
a
ncit:C7057
.
dgn-gda:DGN344845a1259cb3be9cb4b4d1d86bb747
sio:SIO_000628
miriam-gene:9378
,
lld:C0036341
;
a
sio:SIO_001121
.
}
dgn-np:NP730481.RA7ecRrl1grL78LYAg2019S0Ht14TVnox2pKYPZNGEzFA130_provenance
{
dgn-np:NP730481.RA7ecRrl1grL78LYAg2019S0Ht14TVnox2pKYPZNGEzFA130_assertion
dcterms:description
"[There is evidence both for an increased burden of CNVs in schizophrenia and that risk is conferred by specific large deletions at 1q21.1 and at 15q13.2 and by deletions of NRXN1 which encodes the synaptic scaffolding protein neurexin 1.]. 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:19345090
;
prov:wasDerivedFrom
dgn-void:befree-2016
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-2016
pav:importedOn
"2016-02-19"^^
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:NP730481.RA7ecRrl1grL78LYAg2019S0Ht14TVnox2pKYPZNGEzFA130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:47:16+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:disgenetv3.0rdf
;
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
"v4.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v4.0.0" .
}