@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP725514.RAGaiOJiAIcnJI8vQh0krnk8mBlR4CQHeWJViTy2RqqrY
> .
@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:NP725514.RAGaiOJiAIcnJI8vQh0krnk8mBlR4CQHeWJViTy2RqqrY130_head
{
this:
np:hasAssertion
dgn-np:NP725514.RAGaiOJiAIcnJI8vQh0krnk8mBlR4CQHeWJViTy2RqqrY130_assertion
;
np:hasProvenance
dgn-np:NP725514.RAGaiOJiAIcnJI8vQh0krnk8mBlR4CQHeWJViTy2RqqrY130_provenance
;
np:hasPublicationInfo
dgn-np:NP725514.RAGaiOJiAIcnJI8vQh0krnk8mBlR4CQHeWJViTy2RqqrY130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP725514.RAGaiOJiAIcnJI8vQh0krnk8mBlR4CQHeWJViTy2RqqrY130_assertion
a
np:Assertion
.
dgn-np:NP725514.RAGaiOJiAIcnJI8vQh0krnk8mBlR4CQHeWJViTy2RqqrY130_provenance
a
np:Provenance
.
dgn-np:NP725514.RAGaiOJiAIcnJI8vQh0krnk8mBlR4CQHeWJViTy2RqqrY130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP725514.RAGaiOJiAIcnJI8vQh0krnk8mBlR4CQHeWJViTy2RqqrY130_assertion
{
miriam-gene:246319
a
ncit:C16612
.
lld:C0025322
a
ncit:C7057
.
dgn-gda:DGNf731e0d5c2ba4ac2d871df79ba86d40b
sio:SIO_000628
miriam-gene:246319
,
lld:C0025322
;
a
sio:SIO_001121
.
}
dgn-np:NP725514.RAGaiOJiAIcnJI8vQh0krnk8mBlR4CQHeWJViTy2RqqrY130_provenance
{
dgn-np:NP725514.RAGaiOJiAIcnJI8vQh0krnk8mBlR4CQHeWJViTy2RqqrY130_assertion
dcterms:description
"[Type 1 diabetes, alopecia, vitiligo, ectodermal dystrophy, celiac disease and other intestinal dysfunctions, chronic atrophic gastritis, chronic active hepatitis, autoimmune thyroid disorders, pernicious anemia and premature ovarian failure are other rare associated diseases although other conditions have been associated with APECED.]. 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:23000069
;
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:NP725514.RAGaiOJiAIcnJI8vQh0krnk8mBlR4CQHeWJViTy2RqqrY130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:20+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" .
}