@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP708439.RAvb3i_msTmoNl_3KBcEORojfqSQTncgkO_wv_hNsGUSk
> .
@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:NP708439.RAvb3i_msTmoNl_3KBcEORojfqSQTncgkO_wv_hNsGUSk130_head
{
this:
np:hasAssertion
dgn-np:NP708439.RAvb3i_msTmoNl_3KBcEORojfqSQTncgkO_wv_hNsGUSk130_assertion
;
np:hasProvenance
dgn-np:NP708439.RAvb3i_msTmoNl_3KBcEORojfqSQTncgkO_wv_hNsGUSk130_provenance
;
np:hasPublicationInfo
dgn-np:NP708439.RAvb3i_msTmoNl_3KBcEORojfqSQTncgkO_wv_hNsGUSk130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP708439.RAvb3i_msTmoNl_3KBcEORojfqSQTncgkO_wv_hNsGUSk130_assertion
a
np:Assertion
.
dgn-np:NP708439.RAvb3i_msTmoNl_3KBcEORojfqSQTncgkO_wv_hNsGUSk130_provenance
a
np:Provenance
.
dgn-np:NP708439.RAvb3i_msTmoNl_3KBcEORojfqSQTncgkO_wv_hNsGUSk130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP708439.RAvb3i_msTmoNl_3KBcEORojfqSQTncgkO_wv_hNsGUSk130_assertion
{
miriam-gene:8542
a
ncit:C16612
.
lld:C0085580
a
ncit:C7057
.
dgn-gda:DGNf5039c8a70620e920bf8a43a7e56286f
sio:SIO_000628
miriam-gene:8542
,
lld:C0085580
;
a
sio:SIO_001121
.
}
dgn-np:NP708439.RAvb3i_msTmoNl_3KBcEORojfqSQTncgkO_wv_hNsGUSk130_provenance
{
dgn-np:NP708439.RAvb3i_msTmoNl_3KBcEORojfqSQTncgkO_wv_hNsGUSk130_assertion
dcterms:description
"[Apolipoprotein L1 (APOL1) gene association studies and results of the African American Study of Kidney Disease and Hypertension are disproving the longstanding concept that mild to moderate essential hypertension contributes substantially to end-stage renal disease susceptibility in African Americans.]. 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:22068337
;
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:NP708439.RAvb3i_msTmoNl_3KBcEORojfqSQTncgkO_wv_hNsGUSk130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:10+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" .
}