@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP635816.RAz_I7mgTSfWJdm0Mk7UuQfY--Qaeqx0Q36TXfbjnygqg
> .
@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:NP635816.RAz_I7mgTSfWJdm0Mk7UuQfY--Qaeqx0Q36TXfbjnygqg130_head
{
this:
np:hasAssertion
dgn-np:NP635816.RAz_I7mgTSfWJdm0Mk7UuQfY--Qaeqx0Q36TXfbjnygqg130_assertion
;
np:hasProvenance
dgn-np:NP635816.RAz_I7mgTSfWJdm0Mk7UuQfY--Qaeqx0Q36TXfbjnygqg130_provenance
;
np:hasPublicationInfo
dgn-np:NP635816.RAz_I7mgTSfWJdm0Mk7UuQfY--Qaeqx0Q36TXfbjnygqg130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP635816.RAz_I7mgTSfWJdm0Mk7UuQfY--Qaeqx0Q36TXfbjnygqg130_assertion
a
np:Assertion
.
dgn-np:NP635816.RAz_I7mgTSfWJdm0Mk7UuQfY--Qaeqx0Q36TXfbjnygqg130_provenance
a
np:Provenance
.
dgn-np:NP635816.RAz_I7mgTSfWJdm0Mk7UuQfY--Qaeqx0Q36TXfbjnygqg130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP635816.RAz_I7mgTSfWJdm0Mk7UuQfY--Qaeqx0Q36TXfbjnygqg130_assertion
{
miriam-gene:3075
a
ncit:C16612
.
lld:C2316810
a
ncit:C7057
.
dgn-gda:DGNaefe82d693f488ba0e94bd044d555f35
sio:SIO_000628
miriam-gene:3075
,
lld:C2316810
;
a
sio:SIO_001121
.
}
dgn-np:NP635816.RAz_I7mgTSfWJdm0Mk7UuQfY--Qaeqx0Q36TXfbjnygqg130_provenance
{
dgn-np:NP635816.RAz_I7mgTSfWJdm0Mk7UuQfY--Qaeqx0Q36TXfbjnygqg130_assertion
dcterms:description
"[Recurrent haemolytic uraemic syndrome (HUS) is a genetic form of thrombotic microangiopathy that is mostly associated with low activity of complement factor H. The disorder usually develops in families, leads to end stage renal disease, and invariably recurs after kidney transplantation.]. 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:12020532
;
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:NP635816.RAz_I7mgTSfWJdm0Mk7UuQfY--Qaeqx0Q36TXfbjnygqg130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:23+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" .
}