@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP563723.RAZ7sKZxFZ0RTrRh6fcIa4uMyribu_OABRTkK681WWguk
> .
@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:NP563723.RAZ7sKZxFZ0RTrRh6fcIa4uMyribu_OABRTkK681WWguk130_head
{
this:
np:hasAssertion
dgn-np:NP563723.RAZ7sKZxFZ0RTrRh6fcIa4uMyribu_OABRTkK681WWguk130_assertion
;
np:hasProvenance
dgn-np:NP563723.RAZ7sKZxFZ0RTrRh6fcIa4uMyribu_OABRTkK681WWguk130_provenance
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np:hasPublicationInfo
dgn-np:NP563723.RAZ7sKZxFZ0RTrRh6fcIa4uMyribu_OABRTkK681WWguk130_publicationInfo
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a
np:Nanopublication
.
dgn-np:NP563723.RAZ7sKZxFZ0RTrRh6fcIa4uMyribu_OABRTkK681WWguk130_assertion
a
np:Assertion
.
dgn-np:NP563723.RAZ7sKZxFZ0RTrRh6fcIa4uMyribu_OABRTkK681WWguk130_provenance
a
np:Provenance
.
dgn-np:NP563723.RAZ7sKZxFZ0RTrRh6fcIa4uMyribu_OABRTkK681WWguk130_publicationInfo
a
np:PublicationInfo
.
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dgn-np:NP563723.RAZ7sKZxFZ0RTrRh6fcIa4uMyribu_OABRTkK681WWguk130_assertion
{
miriam-gene:1493
a
ncit:C16612
.
lld:C0043117
a
ncit:C7057
.
dgn-gda:DGN113711d87e66e680d6c02a752cf037dc
sio:SIO_000628
miriam-gene:1493
,
lld:C0043117
;
a
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.
}
dgn-np:NP563723.RAZ7sKZxFZ0RTrRh6fcIa4uMyribu_OABRTkK681WWguk130_provenance
{
dgn-np:NP563723.RAZ7sKZxFZ0RTrRh6fcIa4uMyribu_OABRTkK681WWguk130_assertion
dcterms:description
"[In the present study we have examined the prevalence of the A and G alleles of the CTLA-4 gene in 50 patients with autoimmune hemolytic anemia (AIHA), of which 20 had idiopathic AIHA and 30 had AIHA and chronic lymphocytic leukemia (CLL), and in 60 patients with immune thrombocytopenic purpura (ITP).]. 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:12555221
;
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 .
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dgn-np:NP563723.RAZ7sKZxFZ0RTrRh6fcIa4uMyribu_OABRTkK681WWguk130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:40+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
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pav:authoredBy
<
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> , <
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
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