@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP344177.RADcxGoWfb-_AT1hmo2SdnUgbasAOdALN2mUlo6pvM5Ak
> .
@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:NP344177.RADcxGoWfb-_AT1hmo2SdnUgbasAOdALN2mUlo6pvM5Ak130_head
{
this:
np:hasAssertion
dgn-np:NP344177.RADcxGoWfb-_AT1hmo2SdnUgbasAOdALN2mUlo6pvM5Ak130_assertion
;
np:hasProvenance
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;
np:hasPublicationInfo
dgn-np:NP344177.RADcxGoWfb-_AT1hmo2SdnUgbasAOdALN2mUlo6pvM5Ak130_publicationInfo
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a
np:Nanopublication
.
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a
np:Assertion
.
dgn-np:NP344177.RADcxGoWfb-_AT1hmo2SdnUgbasAOdALN2mUlo6pvM5Ak130_provenance
a
np:Provenance
.
dgn-np:NP344177.RADcxGoWfb-_AT1hmo2SdnUgbasAOdALN2mUlo6pvM5Ak130_publicationInfo
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.
}
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{
miriam-gene:9378
a
ncit:C16612
.
lld:C1510586
a
ncit:C7057
.
dgn-gda:DGNa8562284ab9a293c279f8d4eb89ba83d
sio:SIO_000628
miriam-gene:9378
,
lld:C1510586
;
a
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.
}
dgn-np:NP344177.RADcxGoWfb-_AT1hmo2SdnUgbasAOdALN2mUlo6pvM5Ak130_provenance
{
dgn-np:NP344177.RADcxGoWfb-_AT1hmo2SdnUgbasAOdALN2mUlo6pvM5Ak130_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
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;
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:NP344177.RADcxGoWfb-_AT1hmo2SdnUgbasAOdALN2mUlo6pvM5Ak130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:22+02:00"^^
xsd:dateTime
;
dcterms:rights
<
http://opendatacommons.org/licenses/odbl/1.0/
> ;
dcterms:rightsHolder
dgn-void:IBIGroup
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dcterms:subject
sio:SIO_000983
;
prv:usedData
dgn-void:disgenetrdf
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pav:authoredBy
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> , <
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http://orcid.org/0000-0002-9383-528X
> , <
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http://orcid.org/0000-0003-1244-7654
> ;
pav:createdBy
<
http://orcid.org/0000-0003-0169-8159
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pav:version
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