@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP698194.RAL81enmoZsdAwjIKwowzv6UMoykvH2j1PNp7C8M3AWG8
> .
@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/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@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/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v4.0.0/void/
> .
dgn-np:NP698194.RAL81enmoZsdAwjIKwowzv6UMoykvH2j1PNp7C8M3AWG8130_head
{
this:
np:hasAssertion
dgn-np:NP698194.RAL81enmoZsdAwjIKwowzv6UMoykvH2j1PNp7C8M3AWG8130_assertion
;
np:hasProvenance
dgn-np:NP698194.RAL81enmoZsdAwjIKwowzv6UMoykvH2j1PNp7C8M3AWG8130_provenance
;
np:hasPublicationInfo
dgn-np:NP698194.RAL81enmoZsdAwjIKwowzv6UMoykvH2j1PNp7C8M3AWG8130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP698194.RAL81enmoZsdAwjIKwowzv6UMoykvH2j1PNp7C8M3AWG8130_assertion
a
np:Assertion
.
dgn-np:NP698194.RAL81enmoZsdAwjIKwowzv6UMoykvH2j1PNp7C8M3AWG8130_provenance
a
np:Provenance
.
dgn-np:NP698194.RAL81enmoZsdAwjIKwowzv6UMoykvH2j1PNp7C8M3AWG8130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP698194.RAL81enmoZsdAwjIKwowzv6UMoykvH2j1PNp7C8M3AWG8130_assertion
{
miriam-gene:4627
a
ncit:C16612
.
lld:C0022658
a
ncit:C7057
.
dgn-gda:DGNf94e6c78ef8dd3e8480006e4266658c0
sio:SIO_000628
miriam-gene:4627
,
lld:C0022658
;
a
sio:SIO_001121
.
}
dgn-np:NP698194.RAL81enmoZsdAwjIKwowzv6UMoykvH2j1PNp7C8M3AWG8130_provenance
{
dgn-np:NP698194.RAL81enmoZsdAwjIKwowzv6UMoykvH2j1PNp7C8M3AWG8130_assertion
dcterms:description
"[These new data demonstrate that much of the excess risk of ESRD in African American individuals is attributable to an MYH9 risk haplotype and suggest that hypertension may cause progressive kidney disease only in genetically susceptible individuals or be the result of a primary renal disease.]. 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:18923054
;
prov:wasDerivedFrom
dgn-void:befree-2016
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-2016
pav:importedOn
"2016-02-19"^^
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:NP698194.RAL81enmoZsdAwjIKwowzv6UMoykvH2j1PNp7C8M3AWG8130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:47:01+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:disgenetv3.0rdf
;
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
"v4.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v4.0.0" .
}