@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP645994.RANX-IzgHW2AXb2nMVw_NbgWiJEW-kxiFNvNVSdHi7tgQ
> .
@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:NP645994.RANX-IzgHW2AXb2nMVw_NbgWiJEW-kxiFNvNVSdHi7tgQ130_head
{
this:
np:hasAssertion
dgn-np:NP645994.RANX-IzgHW2AXb2nMVw_NbgWiJEW-kxiFNvNVSdHi7tgQ130_assertion
;
np:hasProvenance
dgn-np:NP645994.RANX-IzgHW2AXb2nMVw_NbgWiJEW-kxiFNvNVSdHi7tgQ130_provenance
;
np:hasPublicationInfo
dgn-np:NP645994.RANX-IzgHW2AXb2nMVw_NbgWiJEW-kxiFNvNVSdHi7tgQ130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP645994.RANX-IzgHW2AXb2nMVw_NbgWiJEW-kxiFNvNVSdHi7tgQ130_assertion
a
np:Assertion
.
dgn-np:NP645994.RANX-IzgHW2AXb2nMVw_NbgWiJEW-kxiFNvNVSdHi7tgQ130_provenance
a
np:Provenance
.
dgn-np:NP645994.RANX-IzgHW2AXb2nMVw_NbgWiJEW-kxiFNvNVSdHi7tgQ130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP645994.RANX-IzgHW2AXb2nMVw_NbgWiJEW-kxiFNvNVSdHi7tgQ130_assertion
{
miriam-gene:3359
a
ncit:C16612
.
lld:C1970945
a
ncit:C7057
.
dgn-gda:DGN6433da7362ce458378d6a499b545e9a1
sio:SIO_000628
miriam-gene:3359
,
lld:C1970945
;
a
sio:SIO_001121
.
}
dgn-np:NP645994.RANX-IzgHW2AXb2nMVw_NbgWiJEW-kxiFNvNVSdHi7tgQ130_provenance
{
dgn-np:NP645994.RANX-IzgHW2AXb2nMVw_NbgWiJEW-kxiFNvNVSdHi7tgQ130_assertion
dcterms:description
"[Three single nucleotide polymorphisms (SNPs) in the HTR3A and HTR3B genes (rs1062613, rs1176744 and rs3831455) have been associated with bipolar affective disorder (BPAD) in pilot studies, and all of them are of functional relevance.]. 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:22832903
;
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:NP645994.RANX-IzgHW2AXb2nMVw_NbgWiJEW-kxiFNvNVSdHi7tgQ130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:29+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" .
}