@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP295061.RAbboOnSVK--VTusCIoWceuv6yCN1D3A6hVlot0Zb6NtA
> .
@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:NP295061.RAbboOnSVK--VTusCIoWceuv6yCN1D3A6hVlot0Zb6NtA130_head
{
this:
np:hasAssertion
dgn-np:NP295061.RAbboOnSVK--VTusCIoWceuv6yCN1D3A6hVlot0Zb6NtA130_assertion
;
np:hasProvenance
dgn-np:NP295061.RAbboOnSVK--VTusCIoWceuv6yCN1D3A6hVlot0Zb6NtA130_provenance
;
np:hasPublicationInfo
dgn-np:NP295061.RAbboOnSVK--VTusCIoWceuv6yCN1D3A6hVlot0Zb6NtA130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP295061.RAbboOnSVK--VTusCIoWceuv6yCN1D3A6hVlot0Zb6NtA130_assertion
a
np:Assertion
.
dgn-np:NP295061.RAbboOnSVK--VTusCIoWceuv6yCN1D3A6hVlot0Zb6NtA130_provenance
a
np:Provenance
.
dgn-np:NP295061.RAbboOnSVK--VTusCIoWceuv6yCN1D3A6hVlot0Zb6NtA130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP295061.RAbboOnSVK--VTusCIoWceuv6yCN1D3A6hVlot0Zb6NtA130_assertion
{
miriam-gene:8266
a
ncit:C16612
.
lld:C0022353
a
ncit:C7057
.
dgn-gda:DGNdd4c48fe5a0016dbef34906bdf9c689e
sio:SIO_000628
miriam-gene:8266
,
lld:C0022353
;
a
sio:SIO_001121
.
}
dgn-np:NP295061.RAbboOnSVK--VTusCIoWceuv6yCN1D3A6hVlot0Zb6NtA130_provenance
{
dgn-np:NP295061.RAbboOnSVK--VTusCIoWceuv6yCN1D3A6hVlot0Zb6NtA130_assertion
dcterms:description
"[Single point mutations were also found in G6PD Metaponto (Southern Italy) and in G6PD Ilesha (Nigeria), which are asymptomatic, and in G6PD Chatham, which was observed in an Indian boy with neonatal jaundice.]. 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:3393536
;
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:NP295061.RAbboOnSVK--VTusCIoWceuv6yCN1D3A6hVlot0Zb6NtA130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:47+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" .
}