@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP573784.RAZrQ2HUd4-gfRXiVSBoW5YDfr3XPP4p3UFQ6LRlyD9pY
> .
@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:NP573784.RAZrQ2HUd4-gfRXiVSBoW5YDfr3XPP4p3UFQ6LRlyD9pY130_head
{
this:
np:hasAssertion
dgn-np:NP573784.RAZrQ2HUd4-gfRXiVSBoW5YDfr3XPP4p3UFQ6LRlyD9pY130_assertion
;
np:hasProvenance
dgn-np:NP573784.RAZrQ2HUd4-gfRXiVSBoW5YDfr3XPP4p3UFQ6LRlyD9pY130_provenance
;
np:hasPublicationInfo
dgn-np:NP573784.RAZrQ2HUd4-gfRXiVSBoW5YDfr3XPP4p3UFQ6LRlyD9pY130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP573784.RAZrQ2HUd4-gfRXiVSBoW5YDfr3XPP4p3UFQ6LRlyD9pY130_assertion
a
np:Assertion
.
dgn-np:NP573784.RAZrQ2HUd4-gfRXiVSBoW5YDfr3XPP4p3UFQ6LRlyD9pY130_provenance
a
np:Provenance
.
dgn-np:NP573784.RAZrQ2HUd4-gfRXiVSBoW5YDfr3XPP4p3UFQ6LRlyD9pY130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP573784.RAZrQ2HUd4-gfRXiVSBoW5YDfr3XPP4p3UFQ6LRlyD9pY130_assertion
{
miriam-gene:23771
a
ncit:C16612
.
lld:C0020538
a
ncit:C7057
.
dgn-gda:DGNf81563e66a2c2141834f1adf35ef5f22
sio:SIO_000628
miriam-gene:23771
,
lld:C0020538
;
a
sio:SIO_001121
.
}
dgn-np:NP573784.RAZrQ2HUd4-gfRXiVSBoW5YDfr3XPP4p3UFQ6LRlyD9pY130_provenance
{
dgn-np:NP573784.RAZrQ2HUd4-gfRXiVSBoW5YDfr3XPP4p3UFQ6LRlyD9pY130_assertion
dcterms:description
"[Apart from a more frequent family history of hypertension in patients with allograft DN compared with those without allograft DN, known risk factors for the development of native DN did not significantly differ among patients in the four cohorts.]. 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:12544873
;
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:NP573784.RAZrQ2HUd4-gfRXiVSBoW5YDfr3XPP4p3UFQ6LRlyD9pY130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:46+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" .
}