@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP532057.RA16rS11_ygS2VzjprkwYo8kDXJtwQShqU3jH8nGrqU_4
> .
@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#
> .
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{
this:
np:hasAssertion
dgn-np:NP532057.RA16rS11_ygS2VzjprkwYo8kDXJtwQShqU3jH8nGrqU_4130_assertion
;
np:hasProvenance
dgn-np:NP532057.RA16rS11_ygS2VzjprkwYo8kDXJtwQShqU3jH8nGrqU_4130_provenance
;
np:hasPublicationInfo
dgn-np:NP532057.RA16rS11_ygS2VzjprkwYo8kDXJtwQShqU3jH8nGrqU_4130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP532057.RA16rS11_ygS2VzjprkwYo8kDXJtwQShqU3jH8nGrqU_4130_assertion
a
np:Assertion
.
dgn-np:NP532057.RA16rS11_ygS2VzjprkwYo8kDXJtwQShqU3jH8nGrqU_4130_provenance
a
np:Provenance
.
dgn-np:NP532057.RA16rS11_ygS2VzjprkwYo8kDXJtwQShqU3jH8nGrqU_4130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP532057.RA16rS11_ygS2VzjprkwYo8kDXJtwQShqU3jH8nGrqU_4130_assertion
{
miriam-gene:81494
a
ncit:C16612
.
lld:C0019061
a
ncit:C7057
.
dgn-gda:DGN097cdee9d4fff124a7117a0cff237b3f
sio:SIO_000628
miriam-gene:81494
,
lld:C0019061
;
a
sio:SIO_001121
.
}
dgn-np:NP532057.RA16rS11_ygS2VzjprkwYo8kDXJtwQShqU3jH8nGrqU_4130_provenance
{
dgn-np:NP532057.RA16rS11_ygS2VzjprkwYo8kDXJtwQShqU3jH8nGrqU_4130_assertion
dcterms:description
"[In this review, we discuss how studying CFHR5 nephropathy can contribute to our understanding of the role of complement in kidney diseases such as dense deposit disease, C3 glomerulonephritis and atypical haemolytic uraemic syndrome.]. 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:22065842
;
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:NP532057.RA16rS11_ygS2VzjprkwYo8kDXJtwQShqU3jH8nGrqU_4130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:21+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" .
}