@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP641609.RAl30Pwdp_MrJ5-kcnQHPyL1kIdGqcQtl3GTb89NMRzmM
> .
@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:NP641609.RAl30Pwdp_MrJ5-kcnQHPyL1kIdGqcQtl3GTb89NMRzmM130_head
{
this:
np:hasAssertion
dgn-np:NP641609.RAl30Pwdp_MrJ5-kcnQHPyL1kIdGqcQtl3GTb89NMRzmM130_assertion
;
np:hasProvenance
dgn-np:NP641609.RAl30Pwdp_MrJ5-kcnQHPyL1kIdGqcQtl3GTb89NMRzmM130_provenance
;
np:hasPublicationInfo
dgn-np:NP641609.RAl30Pwdp_MrJ5-kcnQHPyL1kIdGqcQtl3GTb89NMRzmM130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP641609.RAl30Pwdp_MrJ5-kcnQHPyL1kIdGqcQtl3GTb89NMRzmM130_assertion
a
np:Assertion
.
dgn-np:NP641609.RAl30Pwdp_MrJ5-kcnQHPyL1kIdGqcQtl3GTb89NMRzmM130_provenance
a
np:Provenance
.
dgn-np:NP641609.RAl30Pwdp_MrJ5-kcnQHPyL1kIdGqcQtl3GTb89NMRzmM130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP641609.RAl30Pwdp_MrJ5-kcnQHPyL1kIdGqcQtl3GTb89NMRzmM130_assertion
{
miriam-gene:2539
a
ncit:C16612
.
lld:C0015702
a
ncit:C7057
.
dgn-gda:DGNce14919d53cf64259ab69927f39152b7
sio:SIO_000628
miriam-gene:2539
,
lld:C0015702
;
a
sio:SIO_001121
.
}
dgn-np:NP641609.RAl30Pwdp_MrJ5-kcnQHPyL1kIdGqcQtl3GTb89NMRzmM130_provenance
{
dgn-np:NP641609.RAl30Pwdp_MrJ5-kcnQHPyL1kIdGqcQtl3GTb89NMRzmM130_assertion
dcterms:description
"[Favism and mild chronic hemolysis characterized the phenotype of the patient with G6PD Sumaré which contrasts with the more severe clinical picture of the patient with G6PD Utrecht and, in addition, that of the patient originally described with G6PD Sumaré.]. 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:14757424
;
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:NP641609.RAl30Pwdp_MrJ5-kcnQHPyL1kIdGqcQtl3GTb89NMRzmM130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:27+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" .
}