@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP897658.RA07d5SkN3xhCu3z7jUp8Q4_DvgI5-KJ5s3_PqN4BZ1EE
> .
@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:NP897658.RA07d5SkN3xhCu3z7jUp8Q4_DvgI5-KJ5s3_PqN4BZ1EE130_head
{
this:
np:hasAssertion
dgn-np:NP897658.RA07d5SkN3xhCu3z7jUp8Q4_DvgI5-KJ5s3_PqN4BZ1EE130_assertion
;
np:hasProvenance
dgn-np:NP897658.RA07d5SkN3xhCu3z7jUp8Q4_DvgI5-KJ5s3_PqN4BZ1EE130_provenance
;
np:hasPublicationInfo
dgn-np:NP897658.RA07d5SkN3xhCu3z7jUp8Q4_DvgI5-KJ5s3_PqN4BZ1EE130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP897658.RA07d5SkN3xhCu3z7jUp8Q4_DvgI5-KJ5s3_PqN4BZ1EE130_assertion
a
np:Assertion
.
dgn-np:NP897658.RA07d5SkN3xhCu3z7jUp8Q4_DvgI5-KJ5s3_PqN4BZ1EE130_provenance
a
np:Provenance
.
dgn-np:NP897658.RA07d5SkN3xhCu3z7jUp8Q4_DvgI5-KJ5s3_PqN4BZ1EE130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP897658.RA07d5SkN3xhCu3z7jUp8Q4_DvgI5-KJ5s3_PqN4BZ1EE130_assertion
{
miriam-gene:3040
a
ncit:C16612
.
lld:C0268731
a
ncit:C7057
.
dgn-gda:DGN172d19bfa7ca6681c4ba3e8a184c3fb5
sio:SIO_000628
miriam-gene:3040
,
lld:C0268731
;
a
sio:SIO_001121
.
}
dgn-np:NP897658.RA07d5SkN3xhCu3z7jUp8Q4_DvgI5-KJ5s3_PqN4BZ1EE130_provenance
{
dgn-np:NP897658.RA07d5SkN3xhCu3z7jUp8Q4_DvgI5-KJ5s3_PqN4BZ1EE130_assertion
dcterms:description
"[To investigate the role of the alpha-globin gene microdeletion and beta-globin gene cluster haplotypes on the degree of glomerular involvement, 76 adult SSA patients (hemoglobin SS) were studied to determine the relationship between these genetic markers and the development of sickle cell glomerulopathy.]. 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:10232687
;
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:NP897658.RA07d5SkN3xhCu3z7jUp8Q4_DvgI5-KJ5s3_PqN4BZ1EE130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:41:11+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" .
}