@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP715309.RAZqQL54wnntml7wa0M4eCkpz6h9jD9gDHaRFSCXVrUWU
> .
@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:NP715309.RAZqQL54wnntml7wa0M4eCkpz6h9jD9gDHaRFSCXVrUWU130_head
{
this:
np:hasAssertion
dgn-np:NP715309.RAZqQL54wnntml7wa0M4eCkpz6h9jD9gDHaRFSCXVrUWU130_assertion
;
np:hasProvenance
dgn-np:NP715309.RAZqQL54wnntml7wa0M4eCkpz6h9jD9gDHaRFSCXVrUWU130_provenance
;
np:hasPublicationInfo
dgn-np:NP715309.RAZqQL54wnntml7wa0M4eCkpz6h9jD9gDHaRFSCXVrUWU130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP715309.RAZqQL54wnntml7wa0M4eCkpz6h9jD9gDHaRFSCXVrUWU130_assertion
a
np:Assertion
.
dgn-np:NP715309.RAZqQL54wnntml7wa0M4eCkpz6h9jD9gDHaRFSCXVrUWU130_provenance
a
np:Provenance
.
dgn-np:NP715309.RAZqQL54wnntml7wa0M4eCkpz6h9jD9gDHaRFSCXVrUWU130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP715309.RAZqQL54wnntml7wa0M4eCkpz6h9jD9gDHaRFSCXVrUWU130_assertion
{
miriam-gene:213
a
ncit:C16612
.
lld:C0022658
a
ncit:C7057
.
dgn-gda:DGNf3b63273b3cc0cb5a84d49add2ddf861
sio:SIO_000628
miriam-gene:213
,
lld:C0022658
;
a
sio:SIO_001121
.
}
dgn-np:NP715309.RAZqQL54wnntml7wa0M4eCkpz6h9jD9gDHaRFSCXVrUWU130_provenance
{
dgn-np:NP715309.RAZqQL54wnntml7wa0M4eCkpz6h9jD9gDHaRFSCXVrUWU130_assertion
dcterms:description
"[Four single nucleotide polymorphisms comprising the major MYH9 E1 risk haplotype were tested for association with estimated glomerular filtration rate (eGFR) and urine albumin:creatinine ratio (ACR) in 2,903 HyperGEN participants (1,458 African Americans (AA) in 895 families and 1,445 European Americans (EA) in 859 families) to determine the role of MYH9 in subclinical nephropathy.]. 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:19153477
;
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:NP715309.RAZqQL54wnntml7wa0M4eCkpz6h9jD9gDHaRFSCXVrUWU130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:47:09+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" .
}