@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP748290.RANRQMQSajVJLfgIo9wvK5mQt_0jIYq5A29i9N3_yg_84
> .
@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:NP748290.RANRQMQSajVJLfgIo9wvK5mQt_0jIYq5A29i9N3_yg_84130_head
{
this:
np:hasAssertion
dgn-np:NP748290.RANRQMQSajVJLfgIo9wvK5mQt_0jIYq5A29i9N3_yg_84130_assertion
;
np:hasProvenance
dgn-np:NP748290.RANRQMQSajVJLfgIo9wvK5mQt_0jIYq5A29i9N3_yg_84130_provenance
;
np:hasPublicationInfo
dgn-np:NP748290.RANRQMQSajVJLfgIo9wvK5mQt_0jIYq5A29i9N3_yg_84130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP748290.RANRQMQSajVJLfgIo9wvK5mQt_0jIYq5A29i9N3_yg_84130_assertion
a
np:Assertion
.
dgn-np:NP748290.RANRQMQSajVJLfgIo9wvK5mQt_0jIYq5A29i9N3_yg_84130_provenance
a
np:Provenance
.
dgn-np:NP748290.RANRQMQSajVJLfgIo9wvK5mQt_0jIYq5A29i9N3_yg_84130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP748290.RANRQMQSajVJLfgIo9wvK5mQt_0jIYq5A29i9N3_yg_84130_assertion
{
miriam-gene:10058
a
ncit:C16612
.
lld:C2919706
a
ncit:C7057
.
dgn-gda:DGN7e63aa0e84b121d6611f8b635c2d2a6d
sio:SIO_000628
miriam-gene:10058
,
lld:C2919706
;
a
sio:SIO_001121
.
}
dgn-np:NP748290.RANRQMQSajVJLfgIo9wvK5mQt_0jIYq5A29i9N3_yg_84130_provenance
{
dgn-np:NP748290.RANRQMQSajVJLfgIo9wvK5mQt_0jIYq5A29i9N3_yg_84130_assertion
dcterms:description
"[Frequencies of the HLA antigens ABC, DR and MT, as well as of the properdin factor alleles were determined in 24 unrelated patients presenting with immune complex mediated idiopathic rapidly progressive glomerulonephritis (RPGN) type II.]. 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:6233449
;
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:NP748290.RANRQMQSajVJLfgIo9wvK5mQt_0jIYq5A29i9N3_yg_84130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:33+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" .
}