@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP413238.RAVAaahq6CRZ3MD-cUrEfNJ_iDZkR5p4RBby2vcVPc86Y
> .
@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:NP413238.RAVAaahq6CRZ3MD-cUrEfNJ_iDZkR5p4RBby2vcVPc86Y130_head
{
this:
np:hasAssertion
dgn-np:NP413238.RAVAaahq6CRZ3MD-cUrEfNJ_iDZkR5p4RBby2vcVPc86Y130_assertion
;
np:hasProvenance
dgn-np:NP413238.RAVAaahq6CRZ3MD-cUrEfNJ_iDZkR5p4RBby2vcVPc86Y130_provenance
;
np:hasPublicationInfo
dgn-np:NP413238.RAVAaahq6CRZ3MD-cUrEfNJ_iDZkR5p4RBby2vcVPc86Y130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP413238.RAVAaahq6CRZ3MD-cUrEfNJ_iDZkR5p4RBby2vcVPc86Y130_assertion
a
np:Assertion
.
dgn-np:NP413238.RAVAaahq6CRZ3MD-cUrEfNJ_iDZkR5p4RBby2vcVPc86Y130_provenance
a
np:Provenance
.
dgn-np:NP413238.RAVAaahq6CRZ3MD-cUrEfNJ_iDZkR5p4RBby2vcVPc86Y130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP413238.RAVAaahq6CRZ3MD-cUrEfNJ_iDZkR5p4RBby2vcVPc86Y130_assertion
{
miriam-gene:3553
a
ncit:C16612
.
lld:C0595905
a
ncit:C7057
.
dgn-gda:DGN8b55b23c9e947607dbb71557b05f5b9e
sio:SIO_000628
miriam-gene:3553
,
lld:C0595905
;
a
sio:SIO_001121
.
}
dgn-np:NP413238.RAVAaahq6CRZ3MD-cUrEfNJ_iDZkR5p4RBby2vcVPc86Y130_provenance
{
dgn-np:NP413238.RAVAaahq6CRZ3MD-cUrEfNJ_iDZkR5p4RBby2vcVPc86Y130_assertion
dcterms:description
"[Interleukin-1 (IL-1) cluster (chromosome 2q13) genetic variability, previously associated with an increased risk both for schizophrenia and for bipolar disorder, has been also associated with gray matter (GM) deficits, ventricular enlargement and hypoactivity of prefrontal cortex in schizophrenia.]. 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:19125864
;
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:NP413238.RAVAaahq6CRZ3MD-cUrEfNJ_iDZkR5p4RBby2vcVPc86Y130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:05+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" .
}