@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP525085.RAmK0vesGAV_oLKgaOpE7rNQV1N5oGUR2jgBcd3nfYj1Y
> .
@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:NP525085.RAmK0vesGAV_oLKgaOpE7rNQV1N5oGUR2jgBcd3nfYj1Y130_head
{
this:
np:hasAssertion
dgn-np:NP525085.RAmK0vesGAV_oLKgaOpE7rNQV1N5oGUR2jgBcd3nfYj1Y130_assertion
;
np:hasProvenance
dgn-np:NP525085.RAmK0vesGAV_oLKgaOpE7rNQV1N5oGUR2jgBcd3nfYj1Y130_provenance
;
np:hasPublicationInfo
dgn-np:NP525085.RAmK0vesGAV_oLKgaOpE7rNQV1N5oGUR2jgBcd3nfYj1Y130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP525085.RAmK0vesGAV_oLKgaOpE7rNQV1N5oGUR2jgBcd3nfYj1Y130_assertion
a
np:Assertion
.
dgn-np:NP525085.RAmK0vesGAV_oLKgaOpE7rNQV1N5oGUR2jgBcd3nfYj1Y130_provenance
a
np:Provenance
.
dgn-np:NP525085.RAmK0vesGAV_oLKgaOpE7rNQV1N5oGUR2jgBcd3nfYj1Y130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP525085.RAmK0vesGAV_oLKgaOpE7rNQV1N5oGUR2jgBcd3nfYj1Y130_assertion
{
miriam-gene:1356
a
ncit:C16612
.
lld:C1858582
a
ncit:C7057
.
dgn-gda:DGN77c9643e8839a549c9ce0d3b203daf84
sio:SIO_000628
miriam-gene:1356
,
lld:C1858582
;
a
sio:SIO_001121
.
}
dgn-np:NP525085.RAmK0vesGAV_oLKgaOpE7rNQV1N5oGUR2jgBcd3nfYj1Y130_provenance
{
dgn-np:NP525085.RAmK0vesGAV_oLKgaOpE7rNQV1N5oGUR2jgBcd3nfYj1Y130_assertion
dcterms:description
"[Ceruloplasmin is involved in iron metabolism, and the findings suggest that hypoceruloplasminemia due to lack of apoceruloplasmin was causally linked to the iron deposition in basal ganglia and other organs, leading to blepharospasm and retinal degeneration.]. 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:3574673
;
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:NP525085.RAmK0vesGAV_oLKgaOpE7rNQV1N5oGUR2jgBcd3nfYj1Y130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:15+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" .
}