@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP675133.RAhjHqT4TOaxurB6G7T3kKPMVOTg0I7sVGPQrqPEy_CoA
> .
@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:NP675133.RAhjHqT4TOaxurB6G7T3kKPMVOTg0I7sVGPQrqPEy_CoA130_head
{
this:
np:hasAssertion
dgn-np:NP675133.RAhjHqT4TOaxurB6G7T3kKPMVOTg0I7sVGPQrqPEy_CoA130_assertion
;
np:hasProvenance
dgn-np:NP675133.RAhjHqT4TOaxurB6G7T3kKPMVOTg0I7sVGPQrqPEy_CoA130_provenance
;
np:hasPublicationInfo
dgn-np:NP675133.RAhjHqT4TOaxurB6G7T3kKPMVOTg0I7sVGPQrqPEy_CoA130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP675133.RAhjHqT4TOaxurB6G7T3kKPMVOTg0I7sVGPQrqPEy_CoA130_assertion
a
np:Assertion
.
dgn-np:NP675133.RAhjHqT4TOaxurB6G7T3kKPMVOTg0I7sVGPQrqPEy_CoA130_provenance
a
np:Provenance
.
dgn-np:NP675133.RAhjHqT4TOaxurB6G7T3kKPMVOTg0I7sVGPQrqPEy_CoA130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP675133.RAhjHqT4TOaxurB6G7T3kKPMVOTg0I7sVGPQrqPEy_CoA130_assertion
{
miriam-gene:493
a
ncit:C16612
.
lld:C0004352
a
ncit:C7057
.
dgn-gda:DGN0d4ce7aeb75f2d8a16340529d3302327
sio:SIO_000628
miriam-gene:493
,
lld:C0004352
;
a
sio:SIO_001121
.
}
dgn-np:NP675133.RAhjHqT4TOaxurB6G7T3kKPMVOTg0I7sVGPQrqPEy_CoA130_provenance
{
dgn-np:NP675133.RAhjHqT4TOaxurB6G7T3kKPMVOTg0I7sVGPQrqPEy_CoA130_assertion
dcterms:description
"[These results provide converging evidence for an association between ATP2B2 gene variants and autism in male subjects, spurring interest into the identification of functional variants, most likely involved in the homeostasis of Ca2+ signaling.]. 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:21757185
;
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:NP675133.RAhjHqT4TOaxurB6G7T3kKPMVOTg0I7sVGPQrqPEy_CoA130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:47+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" .
}