@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP652956.RAToHTQbJh3G9JT3TofaRodkPJ9hu5KZkns5srczxsuPc
> .
@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:NP652956.RAToHTQbJh3G9JT3TofaRodkPJ9hu5KZkns5srczxsuPc130_head
{
this:
np:hasAssertion
dgn-np:NP652956.RAToHTQbJh3G9JT3TofaRodkPJ9hu5KZkns5srczxsuPc130_assertion
;
np:hasProvenance
dgn-np:NP652956.RAToHTQbJh3G9JT3TofaRodkPJ9hu5KZkns5srczxsuPc130_provenance
;
np:hasPublicationInfo
dgn-np:NP652956.RAToHTQbJh3G9JT3TofaRodkPJ9hu5KZkns5srczxsuPc130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP652956.RAToHTQbJh3G9JT3TofaRodkPJ9hu5KZkns5srczxsuPc130_assertion
a
np:Assertion
.
dgn-np:NP652956.RAToHTQbJh3G9JT3TofaRodkPJ9hu5KZkns5srczxsuPc130_provenance
a
np:Provenance
.
dgn-np:NP652956.RAToHTQbJh3G9JT3TofaRodkPJ9hu5KZkns5srczxsuPc130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP652956.RAToHTQbJh3G9JT3TofaRodkPJ9hu5KZkns5srczxsuPc130_assertion
{
miriam-gene:3084
a
ncit:C16612
.
lld:C0595905
a
ncit:C7057
.
dgn-gda:DGN12ecf8c5da87f8bb3f33579c41a47ce4
sio:SIO_000628
miriam-gene:3084
,
lld:C0595905
;
a
sio:SIO_001121
.
}
dgn-np:NP652956.RAToHTQbJh3G9JT3TofaRodkPJ9hu5KZkns5srczxsuPc130_provenance
{
dgn-np:NP652956.RAToHTQbJh3G9JT3TofaRodkPJ9hu5KZkns5srczxsuPc130_assertion
dcterms:description
"[Recently, the gene that encodes neuregulin-1 (NRG1) has been identified as a potential susceptibility gene for schizophrenia, and defects in the expression of erbB3, one of the NRG1 receptors, have been shown to occur in the prefrontal cortex of schizophrenic patients, suggesting that NRG1-erbB signaling is involved in the pathogenesis of 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:15162166
;
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:NP652956.RAToHTQbJh3G9JT3TofaRodkPJ9hu5KZkns5srczxsuPc130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:33+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" .
}