@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP898583.RAdiVgvtmUNnV-AZCgVKazqRZ7488x6aOX7CejICCDjRU
> .
@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:NP898583.RAdiVgvtmUNnV-AZCgVKazqRZ7488x6aOX7CejICCDjRU130_head
{
this:
np:hasAssertion
dgn-np:NP898583.RAdiVgvtmUNnV-AZCgVKazqRZ7488x6aOX7CejICCDjRU130_assertion
;
np:hasProvenance
dgn-np:NP898583.RAdiVgvtmUNnV-AZCgVKazqRZ7488x6aOX7CejICCDjRU130_provenance
;
np:hasPublicationInfo
dgn-np:NP898583.RAdiVgvtmUNnV-AZCgVKazqRZ7488x6aOX7CejICCDjRU130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP898583.RAdiVgvtmUNnV-AZCgVKazqRZ7488x6aOX7CejICCDjRU130_assertion
a
np:Assertion
.
dgn-np:NP898583.RAdiVgvtmUNnV-AZCgVKazqRZ7488x6aOX7CejICCDjRU130_provenance
a
np:Provenance
.
dgn-np:NP898583.RAdiVgvtmUNnV-AZCgVKazqRZ7488x6aOX7CejICCDjRU130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP898583.RAdiVgvtmUNnV-AZCgVKazqRZ7488x6aOX7CejICCDjRU130_assertion
{
miriam-gene:3359
a
ncit:C16612
.
lld:C0525045
a
ncit:C7057
.
dgn-gda:DGNb2bf0ade2f6031fbb8f623a430297d32
sio:SIO_000628
miriam-gene:3359
,
lld:C0525045
;
a
sio:SIO_001121
.
}
dgn-np:NP898583.RAdiVgvtmUNnV-AZCgVKazqRZ7488x6aOX7CejICCDjRU130_provenance
{
dgn-np:NP898583.RAdiVgvtmUNnV-AZCgVKazqRZ7488x6aOX7CejICCDjRU130_assertion
dcterms:description
"[To determine the haplotype block structure in the genomic regions of HTR3A and HTR3B, and to examine whether genetic variations in the region show evidence of association with schizophrenia and affective disorder in the Japanese, we performed haplotype-based case-control analysis using 29 polymorphisms.]. 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:16487942
;
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:NP898583.RAdiVgvtmUNnV-AZCgVKazqRZ7488x6aOX7CejICCDjRU130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:41:12+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" .
}