@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP692889.RAR6UzRFEvRC9Tcc6PTIbKMKd7nNmeERCbGGbfnPCrglU
> .
@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
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np:hasProvenance
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np:hasPublicationInfo
dgn-np:NP692889.RAR6UzRFEvRC9Tcc6PTIbKMKd7nNmeERCbGGbfnPCrglU130_publicationInfo
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a
np:Nanopublication
.
dgn-np:NP692889.RAR6UzRFEvRC9Tcc6PTIbKMKd7nNmeERCbGGbfnPCrglU130_assertion
a
np:Assertion
.
dgn-np:NP692889.RAR6UzRFEvRC9Tcc6PTIbKMKd7nNmeERCbGGbfnPCrglU130_provenance
a
np:Provenance
.
dgn-np:NP692889.RAR6UzRFEvRC9Tcc6PTIbKMKd7nNmeERCbGGbfnPCrglU130_publicationInfo
a
np:PublicationInfo
.
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dgn-np:NP692889.RAR6UzRFEvRC9Tcc6PTIbKMKd7nNmeERCbGGbfnPCrglU130_assertion
{
miriam-gene:3782
a
ncit:C16612
.
lld:C0349204
a
ncit:C7057
.
dgn-gda:DGNe5f5d6f52048a9c59e6cda7eb7767db8
sio:SIO_000628
miriam-gene:3782
,
lld:C0349204
;
a
sio:SIO_001121
.
}
dgn-np:NP692889.RAR6UzRFEvRC9Tcc6PTIbKMKd7nNmeERCbGGbfnPCrglU130_provenance
{
dgn-np:NP692889.RAR6UzRFEvRC9Tcc6PTIbKMKd7nNmeERCbGGbfnPCrglU130_assertion
dcterms:description
"[Our results support the hypothesis that a contribution of the KCNN3 gene to genetic susceptibility to major psychosis and their phenotypic polymorphism may be related to the difference of allele length rather than to the number of CAG repeats.]. 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:12960745
;
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:NP692889.RAR6UzRFEvRC9Tcc6PTIbKMKd7nNmeERCbGGbfnPCrglU130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:01+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
<
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> , <
http://orcid.org/0000-0002-7534-7661
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http://orcid.org/0000-0002-9383-528X
> , <
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> , <
http://orcid.org/0000-0003-1244-7654
> ;
pav:createdBy
<
http://orcid.org/0000-0003-0169-8159
> ;
pav:version
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dgn-void:disgenetrdf
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"v2.1.0" .
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