@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP811447.RAT3ndkDSNKQ83_iHYQFuQMiREiXfFRP5RQZua0lKWd6Y
> .
@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/
> .
dgn-np:NP811447.RAT3ndkDSNKQ83_iHYQFuQMiREiXfFRP5RQZua0lKWd6Y130_head
{
this:
np:hasAssertion
dgn-np:NP811447.RAT3ndkDSNKQ83_iHYQFuQMiREiXfFRP5RQZua0lKWd6Y130_assertion
;
np:hasProvenance
dgn-np:NP811447.RAT3ndkDSNKQ83_iHYQFuQMiREiXfFRP5RQZua0lKWd6Y130_provenance
;
np:hasPublicationInfo
dgn-np:NP811447.RAT3ndkDSNKQ83_iHYQFuQMiREiXfFRP5RQZua0lKWd6Y130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP811447.RAT3ndkDSNKQ83_iHYQFuQMiREiXfFRP5RQZua0lKWd6Y130_assertion
a
np:Assertion
.
dgn-np:NP811447.RAT3ndkDSNKQ83_iHYQFuQMiREiXfFRP5RQZua0lKWd6Y130_provenance
a
np:Provenance
.
dgn-np:NP811447.RAT3ndkDSNKQ83_iHYQFuQMiREiXfFRP5RQZua0lKWd6Y130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP811447.RAT3ndkDSNKQ83_iHYQFuQMiREiXfFRP5RQZua0lKWd6Y130_assertion
{
miriam-gene:8925
a
ncit:C16612
.
lld:C3714756
a
ncit:C7057
.
dgn-gda:DGN70f36c55b0a6b9d46d01bea17b474cb8
sio:SIO_000628
miriam-gene:8925
,
lld:C3714756
;
a
sio:SIO_001121
.
}
dgn-np:NP811447.RAT3ndkDSNKQ83_iHYQFuQMiREiXfFRP5RQZua0lKWd6Y130_provenance
{
dgn-np:NP811447.RAT3ndkDSNKQ83_iHYQFuQMiREiXfFRP5RQZua0lKWd6Y130_assertion
dcterms:description
"[The phenotypic correlation with the mouse Herc1 and Herc2 mutants as well as the phenotypic overlap with Angelman syndrome provide further evidence that pathogenic changes in HERC2 are associated with nonsyndromic intellectual disability, autism, and gait disturbance.]. 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:23065719
;
prov:wasDerivedFrom
dgn-void:befree-20150227
;
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:NP811447.RAT3ndkDSNKQ83_iHYQFuQMiREiXfFRP5RQZua0lKWd6Y130_publicationInfo
{
this:
dcterms:created
"2015-08-25T14:45:51+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:disgenetv3.0rdf
;
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
"v3.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v3.0.0" .
}