@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP518894.RAPdqihiheUCqLZUgNAxjxLWPCu5ikbJIZnyxGeboRPrU
> .
@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:NP518894.RAPdqihiheUCqLZUgNAxjxLWPCu5ikbJIZnyxGeboRPrU130_head
{
this:
np:hasAssertion
dgn-np:NP518894.RAPdqihiheUCqLZUgNAxjxLWPCu5ikbJIZnyxGeboRPrU130_assertion
;
np:hasProvenance
dgn-np:NP518894.RAPdqihiheUCqLZUgNAxjxLWPCu5ikbJIZnyxGeboRPrU130_provenance
;
np:hasPublicationInfo
dgn-np:NP518894.RAPdqihiheUCqLZUgNAxjxLWPCu5ikbJIZnyxGeboRPrU130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP518894.RAPdqihiheUCqLZUgNAxjxLWPCu5ikbJIZnyxGeboRPrU130_assertion
a
np:Assertion
.
dgn-np:NP518894.RAPdqihiheUCqLZUgNAxjxLWPCu5ikbJIZnyxGeboRPrU130_provenance
a
np:Provenance
.
dgn-np:NP518894.RAPdqihiheUCqLZUgNAxjxLWPCu5ikbJIZnyxGeboRPrU130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP518894.RAPdqihiheUCqLZUgNAxjxLWPCu5ikbJIZnyxGeboRPrU130_assertion
{
miriam-gene:475
a
ncit:C16612
.
lld:C0019202
a
ncit:C7057
.
dgn-gda:DGNa74741a96188eaff128a54e94b4e40d9
sio:SIO_000628
miriam-gene:475
,
lld:C0019202
;
a
sio:SIO_001121
.
}
dgn-np:NP518894.RAPdqihiheUCqLZUgNAxjxLWPCu5ikbJIZnyxGeboRPrU130_provenance
{
dgn-np:NP518894.RAPdqihiheUCqLZUgNAxjxLWPCu5ikbJIZnyxGeboRPrU130_assertion
dcterms:description
"[Recently, the gene underlying Wilson disease (ATP7B) as well as copper transport genes hCTR1, hCTR2 and ATOX1 have been excluded as candidates for NICC in man and copper toxicosis in Bedlington terriers.]. 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:10425268
;
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:NP518894.RAPdqihiheUCqLZUgNAxjxLWPCu5ikbJIZnyxGeboRPrU130_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" .
}