@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP120192.RAtfwHFzv9OAsM8bkbY8HuJX8o06cSjFIJQNwNR3k3-3k
> .
@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:NP120192.RAtfwHFzv9OAsM8bkbY8HuJX8o06cSjFIJQNwNR3k3-3k130_head
{
this:
np:hasAssertion
dgn-np:NP120192.RAtfwHFzv9OAsM8bkbY8HuJX8o06cSjFIJQNwNR3k3-3k130_assertion
;
np:hasProvenance
dgn-np:NP120192.RAtfwHFzv9OAsM8bkbY8HuJX8o06cSjFIJQNwNR3k3-3k130_provenance
;
np:hasPublicationInfo
dgn-np:NP120192.RAtfwHFzv9OAsM8bkbY8HuJX8o06cSjFIJQNwNR3k3-3k130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP120192.RAtfwHFzv9OAsM8bkbY8HuJX8o06cSjFIJQNwNR3k3-3k130_assertion
a
np:Assertion
.
dgn-np:NP120192.RAtfwHFzv9OAsM8bkbY8HuJX8o06cSjFIJQNwNR3k3-3k130_provenance
a
np:Provenance
.
dgn-np:NP120192.RAtfwHFzv9OAsM8bkbY8HuJX8o06cSjFIJQNwNR3k3-3k130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP120192.RAtfwHFzv9OAsM8bkbY8HuJX8o06cSjFIJQNwNR3k3-3k130_assertion
{
miriam-gene:3263
a
ncit:C16612
.
lld:C2825055
a
ncit:C7057
.
dgn-gda:DGNb5a9dec66e98c671e99ddbaf849c4ae9
sio:SIO_000628
miriam-gene:3263
,
lld:C2825055
;
a
sio:SIO_001123
.
}
dgn-np:NP120192.RAtfwHFzv9OAsM8bkbY8HuJX8o06cSjFIJQNwNR3k3-3k130_provenance
{
dgn-np:NP120192.RAtfwHFzv9OAsM8bkbY8HuJX8o06cSjFIJQNwNR3k3-3k130_assertion
dcterms:description
"[Hemopexin in minimal change nephropathy relapse subjects may exist in an altered isoform, showing enhanced protease activity as compared with subjects in remission, subjects with other forms of primary glomerulopathy, or healthy controls.]. 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:16079987
;
prov:wasDerivedFrom
dgn-void:lhgdn-20090331
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:lhgdn-20090331
pav:importedOn
"2009-03-31"^^
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:NP120192.RAtfwHFzv9OAsM8bkbY8HuJX8o06cSjFIJQNwNR3k3-3k130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:02+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" .
}