@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP700884.RAgC7V6GxAeTnPLyqulgbL5_ypAEPuL00dYDxUSxiLKJc
> .
@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:NP700884.RAgC7V6GxAeTnPLyqulgbL5_ypAEPuL00dYDxUSxiLKJc130_head
{
this:
np:hasAssertion
dgn-np:NP700884.RAgC7V6GxAeTnPLyqulgbL5_ypAEPuL00dYDxUSxiLKJc130_assertion
;
np:hasProvenance
dgn-np:NP700884.RAgC7V6GxAeTnPLyqulgbL5_ypAEPuL00dYDxUSxiLKJc130_provenance
;
np:hasPublicationInfo
dgn-np:NP700884.RAgC7V6GxAeTnPLyqulgbL5_ypAEPuL00dYDxUSxiLKJc130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP700884.RAgC7V6GxAeTnPLyqulgbL5_ypAEPuL00dYDxUSxiLKJc130_assertion
a
np:Assertion
.
dgn-np:NP700884.RAgC7V6GxAeTnPLyqulgbL5_ypAEPuL00dYDxUSxiLKJc130_provenance
a
np:Provenance
.
dgn-np:NP700884.RAgC7V6GxAeTnPLyqulgbL5_ypAEPuL00dYDxUSxiLKJc130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP700884.RAgC7V6GxAeTnPLyqulgbL5_ypAEPuL00dYDxUSxiLKJc130_assertion
{
miriam-gene:22871
a
ncit:C16612
.
lld:C1510586
a
ncit:C7057
.
dgn-gda:DGN9fc6cf6a900fd29c3acb0e81d3fda5f2
sio:SIO_000628
miriam-gene:22871
,
lld:C1510586
;
a
sio:SIO_001121
.
}
dgn-np:NP700884.RAgC7V6GxAeTnPLyqulgbL5_ypAEPuL00dYDxUSxiLKJc130_provenance
{
dgn-np:NP700884.RAgC7V6GxAeTnPLyqulgbL5_ypAEPuL00dYDxUSxiLKJc130_assertion
dcterms:description
"[A number of genes that undergo radical changes in expression during this transition include candidates for schizophrenia (SZ), bipolar disorder (BD) and autism spectrum disorders (ASD) that function as transcription factors and chromatin modifiers, such as POU3F2 and ZNF804A, and genes coding for cell adhesion proteins implicated in these conditions including NRXN1 and NLGN1.]. 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:21915259
;
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:NP700884.RAgC7V6GxAeTnPLyqulgbL5_ypAEPuL00dYDxUSxiLKJc130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:06+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" .
}