@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP731690.RAXt-g1cSJDKkC9hO6mtlGnBfIaGK53vBLQ_P5ItgQR1A
> .
@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:NP731690.RAXt-g1cSJDKkC9hO6mtlGnBfIaGK53vBLQ_P5ItgQR1A130_head
{
this:
np:hasAssertion
dgn-np:NP731690.RAXt-g1cSJDKkC9hO6mtlGnBfIaGK53vBLQ_P5ItgQR1A130_assertion
;
np:hasProvenance
dgn-np:NP731690.RAXt-g1cSJDKkC9hO6mtlGnBfIaGK53vBLQ_P5ItgQR1A130_provenance
;
np:hasPublicationInfo
dgn-np:NP731690.RAXt-g1cSJDKkC9hO6mtlGnBfIaGK53vBLQ_P5ItgQR1A130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP731690.RAXt-g1cSJDKkC9hO6mtlGnBfIaGK53vBLQ_P5ItgQR1A130_assertion
a
np:Assertion
.
dgn-np:NP731690.RAXt-g1cSJDKkC9hO6mtlGnBfIaGK53vBLQ_P5ItgQR1A130_provenance
a
np:Provenance
.
dgn-np:NP731690.RAXt-g1cSJDKkC9hO6mtlGnBfIaGK53vBLQ_P5ItgQR1A130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP731690.RAXt-g1cSJDKkC9hO6mtlGnBfIaGK53vBLQ_P5ItgQR1A130_assertion
{
miriam-gene:1600
a
ncit:C16612
.
lld:C0004352
a
ncit:C7057
.
dgn-gda:DGNcc40d221d67adcdfdb640cdcf113ccd2
sio:SIO_000628
miriam-gene:1600
,
lld:C0004352
;
a
sio:SIO_001121
.
}
dgn-np:NP731690.RAXt-g1cSJDKkC9hO6mtlGnBfIaGK53vBLQ_P5ItgQR1A130_provenance
{
dgn-np:NP731690.RAXt-g1cSJDKkC9hO6mtlGnBfIaGK53vBLQ_P5ItgQR1A130_assertion
dcterms:description
"[Our findings suggested that variations in DAB1 involved in the Reelin signaling pathway might contribute to genetic susceptibility to autism with Chinese Han decent, supporting the defect in the Reelin signaling pathway as a predisposition factor for autism.]. 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:23333377
;
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:NP731690.RAXt-g1cSJDKkC9hO6mtlGnBfIaGK53vBLQ_P5ItgQR1A130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:24+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" .
}