@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP466255.RAvomoi9Db5AVLmhYm9_SN6TKxiHP0nds2yf04Rz6gwTQ
> .
@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:NP466255.RAvomoi9Db5AVLmhYm9_SN6TKxiHP0nds2yf04Rz6gwTQ130_head
{
this:
np:hasAssertion
dgn-np:NP466255.RAvomoi9Db5AVLmhYm9_SN6TKxiHP0nds2yf04Rz6gwTQ130_assertion
;
np:hasProvenance
dgn-np:NP466255.RAvomoi9Db5AVLmhYm9_SN6TKxiHP0nds2yf04Rz6gwTQ130_provenance
;
np:hasPublicationInfo
dgn-np:NP466255.RAvomoi9Db5AVLmhYm9_SN6TKxiHP0nds2yf04Rz6gwTQ130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP466255.RAvomoi9Db5AVLmhYm9_SN6TKxiHP0nds2yf04Rz6gwTQ130_assertion
a
np:Assertion
.
dgn-np:NP466255.RAvomoi9Db5AVLmhYm9_SN6TKxiHP0nds2yf04Rz6gwTQ130_provenance
a
np:Provenance
.
dgn-np:NP466255.RAvomoi9Db5AVLmhYm9_SN6TKxiHP0nds2yf04Rz6gwTQ130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP466255.RAvomoi9Db5AVLmhYm9_SN6TKxiHP0nds2yf04Rz6gwTQ130_assertion
{
miriam-gene:8924
a
ncit:C16612
.
lld:C0025362
a
ncit:C7057
.
dgn-gda:DGN691ff8c69fe69b3d9f8e15e8ecf5fd2f
sio:SIO_000628
miriam-gene:8924
,
lld:C0025362
;
a
sio:SIO_001121
.
}
dgn-np:NP466255.RAvomoi9Db5AVLmhYm9_SN6TKxiHP0nds2yf04Rz6gwTQ130_provenance
{
dgn-np:NP466255.RAvomoi9Db5AVLmhYm9_SN6TKxiHP0nds2yf04Rz6gwTQ130_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-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:NP466255.RAvomoi9Db5AVLmhYm9_SN6TKxiHP0nds2yf04Rz6gwTQ130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:39+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" .
}