@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP865108.RAKrOFf0-npXQV_WmjYVExZr_Btj3BcP0ouSjDTwDKPJE
> .
@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:NP865108.RAKrOFf0-npXQV_WmjYVExZr_Btj3BcP0ouSjDTwDKPJE130_head
{
this:
np:hasAssertion
dgn-np:NP865108.RAKrOFf0-npXQV_WmjYVExZr_Btj3BcP0ouSjDTwDKPJE130_assertion
;
np:hasProvenance
dgn-np:NP865108.RAKrOFf0-npXQV_WmjYVExZr_Btj3BcP0ouSjDTwDKPJE130_provenance
;
np:hasPublicationInfo
dgn-np:NP865108.RAKrOFf0-npXQV_WmjYVExZr_Btj3BcP0ouSjDTwDKPJE130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP865108.RAKrOFf0-npXQV_WmjYVExZr_Btj3BcP0ouSjDTwDKPJE130_assertion
a
np:Assertion
.
dgn-np:NP865108.RAKrOFf0-npXQV_WmjYVExZr_Btj3BcP0ouSjDTwDKPJE130_provenance
a
np:Provenance
.
dgn-np:NP865108.RAKrOFf0-npXQV_WmjYVExZr_Btj3BcP0ouSjDTwDKPJE130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP865108.RAKrOFf0-npXQV_WmjYVExZr_Btj3BcP0ouSjDTwDKPJE130_assertion
{
miriam-gene:1378
a
ncit:C16612
.
lld:C0011860
a
ncit:C7057
.
dgn-gda:DGN9f844aec50dcf00b3184b88354df4be8
sio:SIO_000628
miriam-gene:1378
,
lld:C0011860
;
a
sio:SIO_001121
.
}
dgn-np:NP865108.RAKrOFf0-npXQV_WmjYVExZr_Btj3BcP0ouSjDTwDKPJE130_provenance
{
dgn-np:NP865108.RAKrOFf0-npXQV_WmjYVExZr_Btj3BcP0ouSjDTwDKPJE130_assertion
dcterms:description
"[The homozygous polymorphisms of CR1 intron 27 and exon 22 (TT and GG) and alleles (T and G) that are associated with low expression of CR1 on red blood cells, conferred significant protection against CM, MOD and malaria deaths.]. 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:23152904
;
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:NP865108.RAKrOFf0-npXQV_WmjYVExZr_Btj3BcP0ouSjDTwDKPJE130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:48+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" .
}