@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP569986.RAvt9lhFivcBJWtoZyPkKPEo70WMTm7-PpnhdpjnVi8rA
> .
@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:NP569986.RAvt9lhFivcBJWtoZyPkKPEo70WMTm7-PpnhdpjnVi8rA130_head
{
this:
np:hasAssertion
dgn-np:NP569986.RAvt9lhFivcBJWtoZyPkKPEo70WMTm7-PpnhdpjnVi8rA130_assertion
;
np:hasProvenance
dgn-np:NP569986.RAvt9lhFivcBJWtoZyPkKPEo70WMTm7-PpnhdpjnVi8rA130_provenance
;
np:hasPublicationInfo
dgn-np:NP569986.RAvt9lhFivcBJWtoZyPkKPEo70WMTm7-PpnhdpjnVi8rA130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP569986.RAvt9lhFivcBJWtoZyPkKPEo70WMTm7-PpnhdpjnVi8rA130_assertion
a
np:Assertion
.
dgn-np:NP569986.RAvt9lhFivcBJWtoZyPkKPEo70WMTm7-PpnhdpjnVi8rA130_provenance
a
np:Provenance
.
dgn-np:NP569986.RAvt9lhFivcBJWtoZyPkKPEo70WMTm7-PpnhdpjnVi8rA130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP569986.RAvt9lhFivcBJWtoZyPkKPEo70WMTm7-PpnhdpjnVi8rA130_assertion
{
miriam-gene:27184
a
ncit:C16612
.
lld:C0036341
a
ncit:C7057
.
dgn-gda:DGN306be339a32f566bf614c43258c4406b
sio:SIO_000628
miriam-gene:27184
,
lld:C0036341
;
a
sio:SIO_001121
.
}
dgn-np:NP569986.RAvt9lhFivcBJWtoZyPkKPEo70WMTm7-PpnhdpjnVi8rA130_provenance
{
dgn-np:NP569986.RAvt9lhFivcBJWtoZyPkKPEo70WMTm7-PpnhdpjnVi8rA130_assertion
dcterms:description
"[The results of karyotypic, clinical, and ERP investigations of this family suggest that the recently described genes DISC1 and DISC2, which are directly disrupted by the breakpoint on chromosome 1, may have a role in the development of a disease phenotype that includes schizophrenia as well as unipolar and bipolar affective disorders.]. 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:11443544
;
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:NP569986.RAvt9lhFivcBJWtoZyPkKPEo70WMTm7-PpnhdpjnVi8rA130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:43+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" .
}