@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP865196.RAzuLvPT0MrvV6BBShz4pohWUDvrlrxxkHtfis_frL8aw
> .
@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/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@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/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v4.0.0/void/
> .
dgn-np:NP865196.RAzuLvPT0MrvV6BBShz4pohWUDvrlrxxkHtfis_frL8aw130_head
{
this:
np:hasAssertion
dgn-np:NP865196.RAzuLvPT0MrvV6BBShz4pohWUDvrlrxxkHtfis_frL8aw130_assertion
;
np:hasProvenance
dgn-np:NP865196.RAzuLvPT0MrvV6BBShz4pohWUDvrlrxxkHtfis_frL8aw130_provenance
;
np:hasPublicationInfo
dgn-np:NP865196.RAzuLvPT0MrvV6BBShz4pohWUDvrlrxxkHtfis_frL8aw130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP865196.RAzuLvPT0MrvV6BBShz4pohWUDvrlrxxkHtfis_frL8aw130_assertion
a
np:Assertion
.
dgn-np:NP865196.RAzuLvPT0MrvV6BBShz4pohWUDvrlrxxkHtfis_frL8aw130_provenance
a
np:Provenance
.
dgn-np:NP865196.RAzuLvPT0MrvV6BBShz4pohWUDvrlrxxkHtfis_frL8aw130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP865196.RAzuLvPT0MrvV6BBShz4pohWUDvrlrxxkHtfis_frL8aw130_assertion
{
miriam-gene:2066
a
ncit:C16612
.
lld:C0036341
a
ncit:C7057
.
dgn-gda:DGN67d817de90317c81dd4e6bf04034d6a1
sio:SIO_000628
miriam-gene:2066
,
lld:C0036341
;
a
sio:SIO_001121
.
}
dgn-np:NP865196.RAzuLvPT0MrvV6BBShz4pohWUDvrlrxxkHtfis_frL8aw130_provenance
{
dgn-np:NP865196.RAzuLvPT0MrvV6BBShz4pohWUDvrlrxxkHtfis_frL8aw130_assertion
dcterms:description
"[We hypothesised that variation in the gene encoding the NRG1 receptor, ErbB4, would also be associated with reduced ALIC integrity and with cognitive impairments characteristic of individuals with bipolar disorder and 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:21232925
;
prov:wasDerivedFrom
dgn-void:befree-2016
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-2016
pav:importedOn
"2016-02-19"^^
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:NP865196.RAzuLvPT0MrvV6BBShz4pohWUDvrlrxxkHtfis_frL8aw130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:48:17+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:disgenetv3.0rdf
;
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
"v4.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v4.0.0" .
}