@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP906136.RAt1Q01IoSLnFtAeCJLeVgClEV-UuiHVPFOHYvf8qGLhA
> .
@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:NP906136.RAt1Q01IoSLnFtAeCJLeVgClEV-UuiHVPFOHYvf8qGLhA130_head
{
this:
np:hasAssertion
dgn-np:NP906136.RAt1Q01IoSLnFtAeCJLeVgClEV-UuiHVPFOHYvf8qGLhA130_assertion
;
np:hasProvenance
dgn-np:NP906136.RAt1Q01IoSLnFtAeCJLeVgClEV-UuiHVPFOHYvf8qGLhA130_provenance
;
np:hasPublicationInfo
dgn-np:NP906136.RAt1Q01IoSLnFtAeCJLeVgClEV-UuiHVPFOHYvf8qGLhA130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP906136.RAt1Q01IoSLnFtAeCJLeVgClEV-UuiHVPFOHYvf8qGLhA130_assertion
a
np:Assertion
.
dgn-np:NP906136.RAt1Q01IoSLnFtAeCJLeVgClEV-UuiHVPFOHYvf8qGLhA130_provenance
a
np:Provenance
.
dgn-np:NP906136.RAt1Q01IoSLnFtAeCJLeVgClEV-UuiHVPFOHYvf8qGLhA130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP906136.RAt1Q01IoSLnFtAeCJLeVgClEV-UuiHVPFOHYvf8qGLhA130_assertion
{
miriam-gene:3358
a
ncit:C16612
.
lld:C0001614
a
ncit:C7057
.
dgn-gda:DGNab8a75bee30585a76afef43afffe386b
sio:SIO_000628
miriam-gene:3358
,
lld:C0001614
;
a
sio:SIO_001121
.
}
dgn-np:NP906136.RAt1Q01IoSLnFtAeCJLeVgClEV-UuiHVPFOHYvf8qGLhA130_provenance
{
dgn-np:NP906136.RAt1Q01IoSLnFtAeCJLeVgClEV-UuiHVPFOHYvf8qGLhA130_assertion
dcterms:description
"[Here we examined RNA editing efficiencies of site A and D of HTR2C in the prefrontal cortex samples of patients with bipolar disorder, schizophrenia, and major depression as well as control subjects by using primer extension combined with denaturing high performance liquid chromatography.]. 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:12853111
;
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:NP906136.RAt1Q01IoSLnFtAeCJLeVgClEV-UuiHVPFOHYvf8qGLhA130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:41:16+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" .
}