@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP794746.RAKlZeVTYV2cDNsxbeWwsZlGLjdWW4MkSLcGd_9K4MHDE
> .
@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/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@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/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v3.0.0/void/
> .
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{
this:
np:hasAssertion
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;
np:hasProvenance
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np:hasPublicationInfo
dgn-np:NP794746.RAKlZeVTYV2cDNsxbeWwsZlGLjdWW4MkSLcGd_9K4MHDE130_publicationInfo
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a
np:Nanopublication
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dgn-np:NP794746.RAKlZeVTYV2cDNsxbeWwsZlGLjdWW4MkSLcGd_9K4MHDE130_assertion
a
np:Assertion
.
dgn-np:NP794746.RAKlZeVTYV2cDNsxbeWwsZlGLjdWW4MkSLcGd_9K4MHDE130_provenance
a
np:Provenance
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{
miriam-gene:8326
a
ncit:C16612
.
lld:C0004352
a
ncit:C7057
.
dgn-gda:DGNe1039e1f2d631085bf213930fd54c5ca
sio:SIO_000628
miriam-gene:8326
,
lld:C0004352
;
a
sio:SIO_001121
.
}
dgn-np:NP794746.RAKlZeVTYV2cDNsxbeWwsZlGLjdWW4MkSLcGd_9K4MHDE130_provenance
{
dgn-np:NP794746.RAKlZeVTYV2cDNsxbeWwsZlGLjdWW4MkSLcGd_9K4MHDE130_assertion
dcterms:description
"[Along with previously reported cases, genotype-phenotype correlation in the patients described here further suggests that haploinsufficiency of HIP1 and YWHAG might cause the severe neurological and neuropsychological deficits including epilepsy and autistic traits, and that the preservation of BAZ1B and FZD9 genes may be related to mild facial features and moderate neuropsychological deficits.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ;
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dgn-void:source_evidence_literature
;
sio:SIO_000772
miriam-pubmed:23756441
;
prov:wasDerivedFrom
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;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-20150227
pav:importedOn
"2015-02-27"^^
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:NP794746.RAKlZeVTYV2cDNsxbeWwsZlGLjdWW4MkSLcGd_9K4MHDE130_publicationInfo
{
this:
dcterms:created
"2015-08-25T14:45:41+02:00"^^
xsd:dateTime
;
dcterms:rights
<
http://opendatacommons.org/licenses/odbl/1.0/
> ;
dcterms:rightsHolder
dgn-void:IBIGroup
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dcterms:subject
sio:SIO_000983
;
prv:usedData
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pav:authoredBy
<
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> , <
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> , <
http://orcid.org/0000-0002-9383-528X
> , <
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> , <
http://orcid.org/0000-0003-1244-7654
> ;
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<
http://orcid.org/0000-0003-0169-8159
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pav:version
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"v3.0.0" .
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