@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP392380.RARdUKwoAIHWyhL6xNpq3qumMW6g8dr_RYT1VuROZSqMA
> .
@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:NP392380.RARdUKwoAIHWyhL6xNpq3qumMW6g8dr_RYT1VuROZSqMA130_head
{
this:
np:hasAssertion
dgn-np:NP392380.RARdUKwoAIHWyhL6xNpq3qumMW6g8dr_RYT1VuROZSqMA130_assertion
;
np:hasProvenance
dgn-np:NP392380.RARdUKwoAIHWyhL6xNpq3qumMW6g8dr_RYT1VuROZSqMA130_provenance
;
np:hasPublicationInfo
dgn-np:NP392380.RARdUKwoAIHWyhL6xNpq3qumMW6g8dr_RYT1VuROZSqMA130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP392380.RARdUKwoAIHWyhL6xNpq3qumMW6g8dr_RYT1VuROZSqMA130_assertion
a
np:Assertion
.
dgn-np:NP392380.RARdUKwoAIHWyhL6xNpq3qumMW6g8dr_RYT1VuROZSqMA130_provenance
a
np:Provenance
.
dgn-np:NP392380.RARdUKwoAIHWyhL6xNpq3qumMW6g8dr_RYT1VuROZSqMA130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP392380.RARdUKwoAIHWyhL6xNpq3qumMW6g8dr_RYT1VuROZSqMA130_assertion
{
miriam-gene:6556
a
ncit:C16612
.
lld:C0003873
a
ncit:C7057
.
dgn-gda:DGNa1426716b06a7ff941b7a76c63ec48c4
sio:SIO_000628
miriam-gene:6556
,
lld:C0003873
;
a
sio:SIO_001121
.
}
dgn-np:NP392380.RARdUKwoAIHWyhL6xNpq3qumMW6g8dr_RYT1VuROZSqMA130_provenance
{
dgn-np:NP392380.RARdUKwoAIHWyhL6xNpq3qumMW6g8dr_RYT1VuROZSqMA130_assertion
dcterms:description
"[Recent genetic studies have found that allelic variants at the human NRAMP1 locus are associated with susceptibility to leprosy (Mycobacterium leprae) and tuberculosis (Mycobacterium tuberculosis) and possibly with the onset of rheumatoid arthritis.]. 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:9719491
;
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:NP392380.RARdUKwoAIHWyhL6xNpq3qumMW6g8dr_RYT1VuROZSqMA130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:53+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" .
}