@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP581567.RAV_XPg9cP4hTxzgOsx7nng0RNPOHWJyoo8CL9Aysizb4
> .
@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#
> .
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{
this:
np:hasAssertion
dgn-np:NP581567.RAV_XPg9cP4hTxzgOsx7nng0RNPOHWJyoo8CL9Aysizb4130_assertion
;
np:hasProvenance
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;
np:hasPublicationInfo
dgn-np:NP581567.RAV_XPg9cP4hTxzgOsx7nng0RNPOHWJyoo8CL9Aysizb4130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP581567.RAV_XPg9cP4hTxzgOsx7nng0RNPOHWJyoo8CL9Aysizb4130_assertion
a
np:Assertion
.
dgn-np:NP581567.RAV_XPg9cP4hTxzgOsx7nng0RNPOHWJyoo8CL9Aysizb4130_provenance
a
np:Provenance
.
dgn-np:NP581567.RAV_XPg9cP4hTxzgOsx7nng0RNPOHWJyoo8CL9Aysizb4130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP581567.RAV_XPg9cP4hTxzgOsx7nng0RNPOHWJyoo8CL9Aysizb4130_assertion
{
miriam-gene:207
a
ncit:C16612
.
lld:C0005586
a
ncit:C7057
.
dgn-gda:DGN971189cdeeaf88ea6dc6e1a2a1315dde
sio:SIO_000628
miriam-gene:207
,
lld:C0005586
;
a
sio:SIO_001121
.
}
dgn-np:NP581567.RAV_XPg9cP4hTxzgOsx7nng0RNPOHWJyoo8CL9Aysizb4130_provenance
{
dgn-np:NP581567.RAV_XPg9cP4hTxzgOsx7nng0RNPOHWJyoo8CL9Aysizb4130_assertion
dcterms:description
"[In conclusion, our findings, by showing the involvement of the AKT1 gene in both schizophrenia and bipolar disorder, support the role of AKT1 in the genetics of both disorders and add support to the view that there is some genetic overlap between them.]. 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:20214684
;
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:NP581567.RAV_XPg9cP4hTxzgOsx7nng0RNPOHWJyoo8CL9Aysizb4130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:50+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" .
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pav:version
"v2.1.0" .
}