@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP427863.RAvbNTcqN0xX-6yuIK_2bUelW7-aFmW_llBeMISiFbPcM
> .
@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:NP427863.RAvbNTcqN0xX-6yuIK_2bUelW7-aFmW_llBeMISiFbPcM130_head
{
this:
np:hasAssertion
dgn-np:NP427863.RAvbNTcqN0xX-6yuIK_2bUelW7-aFmW_llBeMISiFbPcM130_assertion
;
np:hasProvenance
dgn-np:NP427863.RAvbNTcqN0xX-6yuIK_2bUelW7-aFmW_llBeMISiFbPcM130_provenance
;
np:hasPublicationInfo
dgn-np:NP427863.RAvbNTcqN0xX-6yuIK_2bUelW7-aFmW_llBeMISiFbPcM130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP427863.RAvbNTcqN0xX-6yuIK_2bUelW7-aFmW_llBeMISiFbPcM130_assertion
a
np:Assertion
.
dgn-np:NP427863.RAvbNTcqN0xX-6yuIK_2bUelW7-aFmW_llBeMISiFbPcM130_provenance
a
np:Provenance
.
dgn-np:NP427863.RAvbNTcqN0xX-6yuIK_2bUelW7-aFmW_llBeMISiFbPcM130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP427863.RAvbNTcqN0xX-6yuIK_2bUelW7-aFmW_llBeMISiFbPcM130_assertion
{
miriam-gene:10249
a
ncit:C16612
.
lld:C0024534
a
ncit:C7057
.
dgn-gda:DGNc93fe32aeb80b93d9ef26e172efb0c51
sio:SIO_000628
miriam-gene:10249
,
lld:C0024534
;
a
sio:SIO_001121
.
}
dgn-np:NP427863.RAvbNTcqN0xX-6yuIK_2bUelW7-aFmW_llBeMISiFbPcM130_provenance
{
dgn-np:NP427863.RAvbNTcqN0xX-6yuIK_2bUelW7-aFmW_llBeMISiFbPcM130_assertion
dcterms:description
"[Further, the overall haplotype analysis for all the three loci showed predominantly two major haplotypes 'AAC' coding for higher expression of CR1 and 'TGG' haplotype coding for low expression of CR1 level with the former haplotype being significantly associated with CM (P value<0.00619 after Bonferroni correction) compared to mild malaria.]. 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:20951238
;
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:NP427863.RAvbNTcqN0xX-6yuIK_2bUelW7-aFmW_llBeMISiFbPcM130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:13+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" .
}