@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP932794.RAR9WPx6fjM1R1L4uZh79ohyl4yDYi8-gAbgnr2c1DY5A
> .
@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:NP932794.RAR9WPx6fjM1R1L4uZh79ohyl4yDYi8-gAbgnr2c1DY5A130_head
{
this:
np:hasAssertion
dgn-np:NP932794.RAR9WPx6fjM1R1L4uZh79ohyl4yDYi8-gAbgnr2c1DY5A130_assertion
;
np:hasProvenance
dgn-np:NP932794.RAR9WPx6fjM1R1L4uZh79ohyl4yDYi8-gAbgnr2c1DY5A130_provenance
;
np:hasPublicationInfo
dgn-np:NP932794.RAR9WPx6fjM1R1L4uZh79ohyl4yDYi8-gAbgnr2c1DY5A130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP932794.RAR9WPx6fjM1R1L4uZh79ohyl4yDYi8-gAbgnr2c1DY5A130_assertion
a
np:Assertion
.
dgn-np:NP932794.RAR9WPx6fjM1R1L4uZh79ohyl4yDYi8-gAbgnr2c1DY5A130_provenance
a
np:Provenance
.
dgn-np:NP932794.RAR9WPx6fjM1R1L4uZh79ohyl4yDYi8-gAbgnr2c1DY5A130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP932794.RAR9WPx6fjM1R1L4uZh79ohyl4yDYi8-gAbgnr2c1DY5A130_assertion
{
miriam-gene:2539
a
ncit:C16612
.
lld:C0002895
a
ncit:C7057
.
dgn-gda:DGNf4924d6ac07143fcf466a0040282d294
sio:SIO_000628
miriam-gene:2539
,
lld:C0002895
;
a
sio:SIO_001121
.
}
dgn-np:NP932794.RAR9WPx6fjM1R1L4uZh79ohyl4yDYi8-gAbgnr2c1DY5A130_provenance
{
dgn-np:NP932794.RAR9WPx6fjM1R1L4uZh79ohyl4yDYi8-gAbgnr2c1DY5A130_assertion
dcterms:description
"[To study the plasma lipid levels in patients with red cell genetic disorders, we investigated 400 normal individuals, 100 sickle cell disease (SCD) patients, 220 sickle cell heterozygotes (Hb AS), and 100 individuals suffering from glucose-6-phosphate dehydrogenase (G-6-PD) deficiency.]. 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:7563270
;
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:NP932794.RAR9WPx6fjM1R1L4uZh79ohyl4yDYi8-gAbgnr2c1DY5A130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:41:32+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" .
}