@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP477834.RAdnVxxOblggQeljUE7wrNMMpBrXbyalDzndqboMJLKGY
> .
@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/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@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/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v3.0.0/void/
> .
dgn-np:NP477834.RAdnVxxOblggQeljUE7wrNMMpBrXbyalDzndqboMJLKGY130_head
{
this:
np:hasAssertion
dgn-np:NP477834.RAdnVxxOblggQeljUE7wrNMMpBrXbyalDzndqboMJLKGY130_assertion
;
np:hasProvenance
dgn-np:NP477834.RAdnVxxOblggQeljUE7wrNMMpBrXbyalDzndqboMJLKGY130_provenance
;
np:hasPublicationInfo
dgn-np:NP477834.RAdnVxxOblggQeljUE7wrNMMpBrXbyalDzndqboMJLKGY130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP477834.RAdnVxxOblggQeljUE7wrNMMpBrXbyalDzndqboMJLKGY130_assertion
a
np:Assertion
.
dgn-np:NP477834.RAdnVxxOblggQeljUE7wrNMMpBrXbyalDzndqboMJLKGY130_provenance
a
np:Provenance
.
dgn-np:NP477834.RAdnVxxOblggQeljUE7wrNMMpBrXbyalDzndqboMJLKGY130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP477834.RAdnVxxOblggQeljUE7wrNMMpBrXbyalDzndqboMJLKGY130_assertion
{
miriam-gene:3447
a
ncit:C16612
.
lld:C0026918
a
ncit:C7057
.
dgn-gda:DGNb67889a7f95ce8b5844a6eb1e2e89c19
sio:SIO_000628
miriam-gene:3447
,
lld:C0026918
;
a
sio:SIO_001121
.
}
dgn-np:NP477834.RAdnVxxOblggQeljUE7wrNMMpBrXbyalDzndqboMJLKGY130_provenance
{
dgn-np:NP477834.RAdnVxxOblggQeljUE7wrNMMpBrXbyalDzndqboMJLKGY130_assertion
dcterms:description
"[IFN-gammaR1 deficiency is a genetic etiology of Mendelian susceptibility to mycobacterial diseases, and includes two forms of complete recessive deficiency, with or without cell surface expression, and two forms of partial deficiency, dominant or recessive.]. 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:19880857
;
prov:wasDerivedFrom
dgn-void:befree-20150227
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-20150227
pav:importedOn
"2015-02-27"^^
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:NP477834.RAdnVxxOblggQeljUE7wrNMMpBrXbyalDzndqboMJLKGY130_publicationInfo
{
this:
dcterms:created
"2015-08-25T14:42:21+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:disgenetv3.0rdf
;
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
"v3.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v3.0.0" .
}