@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP759579.RAcJMzqVwubFWmfipO5rmHA6bEpA9UolISd-b8PgRenOY
> .
@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:NP759579.RAcJMzqVwubFWmfipO5rmHA6bEpA9UolISd-b8PgRenOY130_head
{
this:
np:hasAssertion
dgn-np:NP759579.RAcJMzqVwubFWmfipO5rmHA6bEpA9UolISd-b8PgRenOY130_assertion
;
np:hasProvenance
dgn-np:NP759579.RAcJMzqVwubFWmfipO5rmHA6bEpA9UolISd-b8PgRenOY130_provenance
;
np:hasPublicationInfo
dgn-np:NP759579.RAcJMzqVwubFWmfipO5rmHA6bEpA9UolISd-b8PgRenOY130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP759579.RAcJMzqVwubFWmfipO5rmHA6bEpA9UolISd-b8PgRenOY130_assertion
a
np:Assertion
.
dgn-np:NP759579.RAcJMzqVwubFWmfipO5rmHA6bEpA9UolISd-b8PgRenOY130_provenance
a
np:Provenance
.
dgn-np:NP759579.RAcJMzqVwubFWmfipO5rmHA6bEpA9UolISd-b8PgRenOY130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP759579.RAcJMzqVwubFWmfipO5rmHA6bEpA9UolISd-b8PgRenOY130_assertion
{
miriam-gene:3594
a
ncit:C16612
.
lld:C0024530
a
ncit:C7057
.
dgn-gda:DGN5814fba98bb14a0acb8a31fd0be7c75a
sio:SIO_000628
miriam-gene:3594
,
lld:C0024530
;
a
sio:SIO_001121
.
}
dgn-np:NP759579.RAcJMzqVwubFWmfipO5rmHA6bEpA9UolISd-b8PgRenOY130_provenance
{
dgn-np:NP759579.RAcJMzqVwubFWmfipO5rmHA6bEpA9UolISd-b8PgRenOY130_assertion
dcterms:description
"[This study has shown strong associations between polymorphisms in the genes of IL12A and IL12RB1 and protection from SMA in Kenyan children, suggesting that human genetic variants of IL12 related genes may significantly contribute to the development of anaemia in malaria patients.]. 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:20350312
;
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:NP759579.RAcJMzqVwubFWmfipO5rmHA6bEpA9UolISd-b8PgRenOY130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:40+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" .
}