@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP491185.RAcYwtHykqQhjXE1ITS2Y-XnhPV90zDBxycaeNF9MDZFc
> .
@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:NP491185.RAcYwtHykqQhjXE1ITS2Y-XnhPV90zDBxycaeNF9MDZFc130_head
{
this:
np:hasAssertion
dgn-np:NP491185.RAcYwtHykqQhjXE1ITS2Y-XnhPV90zDBxycaeNF9MDZFc130_assertion
;
np:hasProvenance
dgn-np:NP491185.RAcYwtHykqQhjXE1ITS2Y-XnhPV90zDBxycaeNF9MDZFc130_provenance
;
np:hasPublicationInfo
dgn-np:NP491185.RAcYwtHykqQhjXE1ITS2Y-XnhPV90zDBxycaeNF9MDZFc130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP491185.RAcYwtHykqQhjXE1ITS2Y-XnhPV90zDBxycaeNF9MDZFc130_assertion
a
np:Assertion
.
dgn-np:NP491185.RAcYwtHykqQhjXE1ITS2Y-XnhPV90zDBxycaeNF9MDZFc130_provenance
a
np:Provenance
.
dgn-np:NP491185.RAcYwtHykqQhjXE1ITS2Y-XnhPV90zDBxycaeNF9MDZFc130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP491185.RAcYwtHykqQhjXE1ITS2Y-XnhPV90zDBxycaeNF9MDZFc130_assertion
{
miriam-gene:81
a
ncit:C16612
.
lld:C0022661
a
ncit:C7057
.
dgn-gda:DGNac48c8bc3680ee29bd6f2fd9354b84a8
sio:SIO_000628
miriam-gene:81
,
lld:C0022661
;
a
sio:SIO_001121
.
}
dgn-np:NP491185.RAcYwtHykqQhjXE1ITS2Y-XnhPV90zDBxycaeNF9MDZFc130_provenance
{
dgn-np:NP491185.RAcYwtHykqQhjXE1ITS2Y-XnhPV90zDBxycaeNF9MDZFc130_assertion
dcterms:description
"[A variation in the MYH9 locus of chromosome 22 has been associated with increased risk for idiopathic FSGS, hypertensive nephrosclerosis and HIVAN and may explain much of the increased risks of ESRD and FSGS among 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:20979964
;
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:NP491185.RAcYwtHykqQhjXE1ITS2Y-XnhPV90zDBxycaeNF9MDZFc130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:53+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" .
}