@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP233155.RANIoSoolaaWlrnAY-1HlYP6rtQgiH_GidT4hattzyK6U
> .
@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:NP233155.RANIoSoolaaWlrnAY-1HlYP6rtQgiH_GidT4hattzyK6U130_head
{
this:
np:hasAssertion
dgn-np:NP233155.RANIoSoolaaWlrnAY-1HlYP6rtQgiH_GidT4hattzyK6U130_assertion
;
np:hasProvenance
dgn-np:NP233155.RANIoSoolaaWlrnAY-1HlYP6rtQgiH_GidT4hattzyK6U130_provenance
;
np:hasPublicationInfo
dgn-np:NP233155.RANIoSoolaaWlrnAY-1HlYP6rtQgiH_GidT4hattzyK6U130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP233155.RANIoSoolaaWlrnAY-1HlYP6rtQgiH_GidT4hattzyK6U130_assertion
a
np:Assertion
.
dgn-np:NP233155.RANIoSoolaaWlrnAY-1HlYP6rtQgiH_GidT4hattzyK6U130_provenance
a
np:Provenance
.
dgn-np:NP233155.RANIoSoolaaWlrnAY-1HlYP6rtQgiH_GidT4hattzyK6U130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP233155.RANIoSoolaaWlrnAY-1HlYP6rtQgiH_GidT4hattzyK6U130_assertion
{
miriam-gene:4627
a
ncit:C16612
.
lld:C0020538
a
ncit:C7057
.
dgn-gda:DGN1d2753a251ea7c43ba83801bcd13d811
sio:SIO_000628
miriam-gene:4627
,
lld:C0020538
;
a
sio:SIO_001121
.
}
dgn-np:NP233155.RANIoSoolaaWlrnAY-1HlYP6rtQgiH_GidT4hattzyK6U130_provenance
{
dgn-np:NP233155.RANIoSoolaaWlrnAY-1HlYP6rtQgiH_GidT4hattzyK6U130_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-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:NP233155.RANIoSoolaaWlrnAY-1HlYP6rtQgiH_GidT4hattzyK6U130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:10+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" .
}