@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP709288.RAcjsY6KpoxAn5XAVhIILdv48U9F9D917AiBXqvNVgflc
> .
@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:NP709288.RAcjsY6KpoxAn5XAVhIILdv48U9F9D917AiBXqvNVgflc130_head
{
this:
np:hasAssertion
dgn-np:NP709288.RAcjsY6KpoxAn5XAVhIILdv48U9F9D917AiBXqvNVgflc130_assertion
;
np:hasProvenance
dgn-np:NP709288.RAcjsY6KpoxAn5XAVhIILdv48U9F9D917AiBXqvNVgflc130_provenance
;
np:hasPublicationInfo
dgn-np:NP709288.RAcjsY6KpoxAn5XAVhIILdv48U9F9D917AiBXqvNVgflc130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP709288.RAcjsY6KpoxAn5XAVhIILdv48U9F9D917AiBXqvNVgflc130_assertion
a
np:Assertion
.
dgn-np:NP709288.RAcjsY6KpoxAn5XAVhIILdv48U9F9D917AiBXqvNVgflc130_provenance
a
np:Provenance
.
dgn-np:NP709288.RAcjsY6KpoxAn5XAVhIILdv48U9F9D917AiBXqvNVgflc130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP709288.RAcjsY6KpoxAn5XAVhIILdv48U9F9D917AiBXqvNVgflc130_assertion
{
miriam-gene:7096
a
ncit:C16612
.
lld:C0041296
a
ncit:C7057
.
dgn-gda:DGN2a7ccfd4a7e72326fc8f7bda23499cc9
sio:SIO_000628
miriam-gene:7096
,
lld:C0041296
;
a
sio:SIO_001121
.
}
dgn-np:NP709288.RAcjsY6KpoxAn5XAVhIILdv48U9F9D917AiBXqvNVgflc130_provenance
{
dgn-np:NP709288.RAcjsY6KpoxAn5XAVhIILdv48U9F9D917AiBXqvNVgflc130_assertion
dcterms:description
"[In the subgroup analysis by ethnicity, Africans and American Hispanic subjects with the TLR1 1805T allele had an increased susceptibility, whereas Asian and European subjects with the TLR2 2258A allele had an increased susceptibility to TB.]. 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:23691034
;
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:NP709288.RAcjsY6KpoxAn5XAVhIILdv48U9F9D917AiBXqvNVgflc130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:11+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" .
}