@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP80545.RAHoRfM6XbXMZeNCypwz6wHCVFbhEQG-6vCruKFm1kUfA
> .
@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:NP80545.RAHoRfM6XbXMZeNCypwz6wHCVFbhEQG-6vCruKFm1kUfA130_head
{
this:
np:hasAssertion
dgn-np:NP80545.RAHoRfM6XbXMZeNCypwz6wHCVFbhEQG-6vCruKFm1kUfA130_assertion
;
np:hasProvenance
dgn-np:NP80545.RAHoRfM6XbXMZeNCypwz6wHCVFbhEQG-6vCruKFm1kUfA130_provenance
;
np:hasPublicationInfo
dgn-np:NP80545.RAHoRfM6XbXMZeNCypwz6wHCVFbhEQG-6vCruKFm1kUfA130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP80545.RAHoRfM6XbXMZeNCypwz6wHCVFbhEQG-6vCruKFm1kUfA130_assertion
a
np:Assertion
.
dgn-np:NP80545.RAHoRfM6XbXMZeNCypwz6wHCVFbhEQG-6vCruKFm1kUfA130_provenance
a
np:Provenance
.
dgn-np:NP80545.RAHoRfM6XbXMZeNCypwz6wHCVFbhEQG-6vCruKFm1kUfA130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP80545.RAHoRfM6XbXMZeNCypwz6wHCVFbhEQG-6vCruKFm1kUfA130_assertion
{
miriam-gene:54658
a
ncit:C16612
.
lld:C0039730
a
ncit:C7057
.
dgn-gda:DGNc0a97edec5792008bdd28febc89b09ae
sio:SIO_000628
miriam-gene:54658
,
lld:C0039730
;
a
sio:SIO_001122
.
}
dgn-np:NP80545.RAHoRfM6XbXMZeNCypwz6wHCVFbhEQG-6vCruKFm1kUfA130_provenance
{
dgn-np:NP80545.RAHoRfM6XbXMZeNCypwz6wHCVFbhEQG-6vCruKFm1kUfA130_assertion
dcterms:description
"[These findings suggest that the coexistence of Gilbert's syndrome in patients with thalassemia intermedia and sickle cell disease may be the cause of the elevated values of unconjugated bilirubin, reducing the possibility of excessive hemolysis in these p]. 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:12850481
;
prov:wasDerivedFrom
dgn-void:gad-20150221
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:gad-20150221
pav:importedOn
"2015-02-21"^^
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:NP80545.RAHoRfM6XbXMZeNCypwz6wHCVFbhEQG-6vCruKFm1kUfA130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:42:24+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" .
}