@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP497358.RA5Xfxrkk0ZZPu364MG9fvRgX7BkJ8H1GdnZm2EWRU_rk
> .
@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:NP497358.RA5Xfxrkk0ZZPu364MG9fvRgX7BkJ8H1GdnZm2EWRU_rk130_head
{
this:
np:hasAssertion
dgn-np:NP497358.RA5Xfxrkk0ZZPu364MG9fvRgX7BkJ8H1GdnZm2EWRU_rk130_assertion
;
np:hasProvenance
dgn-np:NP497358.RA5Xfxrkk0ZZPu364MG9fvRgX7BkJ8H1GdnZm2EWRU_rk130_provenance
;
np:hasPublicationInfo
dgn-np:NP497358.RA5Xfxrkk0ZZPu364MG9fvRgX7BkJ8H1GdnZm2EWRU_rk130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP497358.RA5Xfxrkk0ZZPu364MG9fvRgX7BkJ8H1GdnZm2EWRU_rk130_assertion
a
np:Assertion
.
dgn-np:NP497358.RA5Xfxrkk0ZZPu364MG9fvRgX7BkJ8H1GdnZm2EWRU_rk130_provenance
a
np:Provenance
.
dgn-np:NP497358.RA5Xfxrkk0ZZPu364MG9fvRgX7BkJ8H1GdnZm2EWRU_rk130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP497358.RA5Xfxrkk0ZZPu364MG9fvRgX7BkJ8H1GdnZm2EWRU_rk130_assertion
{
miriam-gene:7473
a
ncit:C16612
.
lld:C0041327
a
ncit:C7057
.
dgn-gda:DGN75f19db978f770b93e4f881b7e3509c8
sio:SIO_000628
miriam-gene:7473
,
lld:C0041327
;
a
sio:SIO_001121
.
}
dgn-np:NP497358.RA5Xfxrkk0ZZPu364MG9fvRgX7BkJ8H1GdnZm2EWRU_rk130_provenance
{
dgn-np:NP497358.RA5Xfxrkk0ZZPu364MG9fvRgX7BkJ8H1GdnZm2EWRU_rk130_assertion
dcterms:description
"[To test this possibility, we examined NRAMP1 variants at the INT4 and D543N loci, as well as their association with severe forms of pulmonary tuberculosis, in 127 patients with active pulmonary tuberculosis and in 91 ethnically matched, healthy control subjects in areas of China where tuberculosis is endemic.]. 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:15825023
;
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:NP497358.RA5Xfxrkk0ZZPu364MG9fvRgX7BkJ8H1GdnZm2EWRU_rk130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:56+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" .
}