@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP205624.RAtSkO2YD256gku0U7k8dvgruJT6A_-8-E33EWiybhvNI
> .
@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:NP205624.RAtSkO2YD256gku0U7k8dvgruJT6A_-8-E33EWiybhvNI130_head
{
this:
np:hasAssertion
dgn-np:NP205624.RAtSkO2YD256gku0U7k8dvgruJT6A_-8-E33EWiybhvNI130_assertion
;
np:hasProvenance
dgn-np:NP205624.RAtSkO2YD256gku0U7k8dvgruJT6A_-8-E33EWiybhvNI130_provenance
;
np:hasPublicationInfo
dgn-np:NP205624.RAtSkO2YD256gku0U7k8dvgruJT6A_-8-E33EWiybhvNI130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP205624.RAtSkO2YD256gku0U7k8dvgruJT6A_-8-E33EWiybhvNI130_assertion
a
np:Assertion
.
dgn-np:NP205624.RAtSkO2YD256gku0U7k8dvgruJT6A_-8-E33EWiybhvNI130_provenance
a
np:Provenance
.
dgn-np:NP205624.RAtSkO2YD256gku0U7k8dvgruJT6A_-8-E33EWiybhvNI130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP205624.RAtSkO2YD256gku0U7k8dvgruJT6A_-8-E33EWiybhvNI130_assertion
{
miriam-gene:1356
a
ncit:C16612
.
lld:C0019202
a
ncit:C7057
.
dgn-gda:DGN8a31b2f6804f9ed455581105303edb09
sio:SIO_000628
miriam-gene:1356
,
lld:C0019202
;
a
sio:SIO_001121
.
}
dgn-np:NP205624.RAtSkO2YD256gku0U7k8dvgruJT6A_-8-E33EWiybhvNI130_provenance
{
dgn-np:NP205624.RAtSkO2YD256gku0U7k8dvgruJT6A_-8-E33EWiybhvNI130_assertion
dcterms:description
"[Wilson disease (WND), an autosomal recessive disorder of copper transport, is characterized by excessive accumulation of intracellular copper in liver and extrahepatic tissues because of impaired biliary copper excretion and disturbed incorporation of copper into ceruloplasmin.]. 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:17587212
;
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:NP205624.RAtSkO2YD256gku0U7k8dvgruJT6A_-8-E33EWiybhvNI130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:53+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" .
}