@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP518675.RAIZ95Ijh-8oEPIQ7c8IhILzuca7UjufDOGWkQNdwDx-8
> .
@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:NP518675.RAIZ95Ijh-8oEPIQ7c8IhILzuca7UjufDOGWkQNdwDx-8130_head
{
this:
np:hasAssertion
dgn-np:NP518675.RAIZ95Ijh-8oEPIQ7c8IhILzuca7UjufDOGWkQNdwDx-8130_assertion
;
np:hasProvenance
dgn-np:NP518675.RAIZ95Ijh-8oEPIQ7c8IhILzuca7UjufDOGWkQNdwDx-8130_provenance
;
np:hasPublicationInfo
dgn-np:NP518675.RAIZ95Ijh-8oEPIQ7c8IhILzuca7UjufDOGWkQNdwDx-8130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP518675.RAIZ95Ijh-8oEPIQ7c8IhILzuca7UjufDOGWkQNdwDx-8130_assertion
a
np:Assertion
.
dgn-np:NP518675.RAIZ95Ijh-8oEPIQ7c8IhILzuca7UjufDOGWkQNdwDx-8130_provenance
a
np:Provenance
.
dgn-np:NP518675.RAIZ95Ijh-8oEPIQ7c8IhILzuca7UjufDOGWkQNdwDx-8130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP518675.RAIZ95Ijh-8oEPIQ7c8IhILzuca7UjufDOGWkQNdwDx-8130_assertion
{
miriam-gene:540
a
ncit:C16612
.
lld:C0302332
a
ncit:C7057
.
dgn-gda:DGNdc9f1881c9e816dd5da76a2896c39ff3
sio:SIO_000628
miriam-gene:540
,
lld:C0302332
;
a
sio:SIO_001121
.
}
dgn-np:NP518675.RAIZ95Ijh-8oEPIQ7c8IhILzuca7UjufDOGWkQNdwDx-8130_provenance
{
dgn-np:NP518675.RAIZ95Ijh-8oEPIQ7c8IhILzuca7UjufDOGWkQNdwDx-8130_assertion
dcterms:description
"[This recessively inherited disorder, similar in many respects to Wilson disease, is of particular interest because the canine Atp7b gene, homologous to ATP7B defective in Wilson disease, is not responsible for canine copper toxicosis as has been expected.]. 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:10585777
;
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:NP518675.RAIZ95Ijh-8oEPIQ7c8IhILzuca7UjufDOGWkQNdwDx-8130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:09+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" .
}