@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP630694.RA_Fk8VW6gjzwQbRHOfvfjgLHO5vOwIopURxG8E53HKX4
> .
@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:NP630694.RA_Fk8VW6gjzwQbRHOfvfjgLHO5vOwIopURxG8E53HKX4130_head
{
this:
np:hasAssertion
dgn-np:NP630694.RA_Fk8VW6gjzwQbRHOfvfjgLHO5vOwIopURxG8E53HKX4130_assertion
;
np:hasProvenance
dgn-np:NP630694.RA_Fk8VW6gjzwQbRHOfvfjgLHO5vOwIopURxG8E53HKX4130_provenance
;
np:hasPublicationInfo
dgn-np:NP630694.RA_Fk8VW6gjzwQbRHOfvfjgLHO5vOwIopURxG8E53HKX4130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP630694.RA_Fk8VW6gjzwQbRHOfvfjgLHO5vOwIopURxG8E53HKX4130_assertion
a
np:Assertion
.
dgn-np:NP630694.RA_Fk8VW6gjzwQbRHOfvfjgLHO5vOwIopURxG8E53HKX4130_provenance
a
np:Provenance
.
dgn-np:NP630694.RA_Fk8VW6gjzwQbRHOfvfjgLHO5vOwIopURxG8E53HKX4130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP630694.RA_Fk8VW6gjzwQbRHOfvfjgLHO5vOwIopURxG8E53HKX4130_assertion
{
miriam-gene:114609
a
ncit:C16612
.
lld:C0041296
a
ncit:C7057
.
dgn-gda:DGN7a9e8427b5e6d124072d31b61b01b7a8
sio:SIO_000628
miriam-gene:114609
,
lld:C0041296
;
a
sio:SIO_001121
.
}
dgn-np:NP630694.RA_Fk8VW6gjzwQbRHOfvfjgLHO5vOwIopURxG8E53HKX4130_provenance
{
dgn-np:NP630694.RA_Fk8VW6gjzwQbRHOfvfjgLHO5vOwIopURxG8E53HKX4130_assertion
dcterms:description
"[A mutation (S180L) in the TLR downstream signal transducer TIRAP has recently been reported to be common in Europeans and Africans and to roughly half the risks of heterogeneous infectious diseases including malaria, tuberculosis, bacteremia, and invasive pneumococal disease in heterozygous mutation carriers.]. 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:19602285
;
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:NP630694.RA_Fk8VW6gjzwQbRHOfvfjgLHO5vOwIopURxG8E53HKX4130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:20+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" .
}