@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP7091.RA_SbuDhiHi60F1TmZTHtyqfb2E56Qrp_Wl-AwvNz8FjY
> .
@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:NP7091.RA_SbuDhiHi60F1TmZTHtyqfb2E56Qrp_Wl-AwvNz8FjY130_head
{
this:
np:hasAssertion
dgn-np:NP7091.RA_SbuDhiHi60F1TmZTHtyqfb2E56Qrp_Wl-AwvNz8FjY130_assertion
;
np:hasProvenance
dgn-np:NP7091.RA_SbuDhiHi60F1TmZTHtyqfb2E56Qrp_Wl-AwvNz8FjY130_provenance
;
np:hasPublicationInfo
dgn-np:NP7091.RA_SbuDhiHi60F1TmZTHtyqfb2E56Qrp_Wl-AwvNz8FjY130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP7091.RA_SbuDhiHi60F1TmZTHtyqfb2E56Qrp_Wl-AwvNz8FjY130_assertion
a
np:Assertion
.
dgn-np:NP7091.RA_SbuDhiHi60F1TmZTHtyqfb2E56Qrp_Wl-AwvNz8FjY130_provenance
a
np:Provenance
.
dgn-np:NP7091.RA_SbuDhiHi60F1TmZTHtyqfb2E56Qrp_Wl-AwvNz8FjY130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP7091.RA_SbuDhiHi60F1TmZTHtyqfb2E56Qrp_Wl-AwvNz8FjY130_assertion
{
miriam-gene:80326
a
ncit:C16612
.
lld:C0796093
a
ncit:C7057
.
dgn-gda:DGNd36b348701ae1f76a59b8052fca7c40a
sio:SIO_000628
miriam-gene:80326
,
lld:C0796093
;
a
sio:SIO_001122
.
}
dgn-np:NP7091.RA_SbuDhiHi60F1TmZTHtyqfb2E56Qrp_Wl-AwvNz8FjY130_provenance
{
dgn-np:NP7091.RA_SbuDhiHi60F1TmZTHtyqfb2E56Qrp_Wl-AwvNz8FjY130_assertion
dcterms:description
"[Recent insights into the role of Wnt10A in tooth development, and the finding of hypodontia in carriers of the autosomal recessive disorder, odontooncychodermal dysplasia, due to mutations in WNT10A (OMIM 257980; OODD), make WNT10A an interesting candidate gene for dental agenesis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ;
wi:evidence
dgn-void:source_evidence_curated
;
sio:SIO_000772
miriam-pubmed:22581971
;
prov:wasDerivedFrom
dgn-void:uniprot-20130724
;
prov:wasGeneratedBy
eco:ECO_0000218
.
dgn-void:source_evidence_curated
a
eco:ECO_0000205
;
rdfs:comment
"Gene-disease associations manually curated."@en ;
rdfs:label
"DisGeNET evidence - CURATED"@en .
dgn-void:uniprot-20130724
pav:importedOn
"2013-07-24"^^
xsd:date
.
}
dgn-np:NP7091.RA_SbuDhiHi60F1TmZTHtyqfb2E56Qrp_Wl-AwvNz8FjY130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:01+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" .
}