@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP860459.RAmf3oNpEOx30P-JDxko_hugAOv7Zx0Ufa1eq9EXqK0HQ
> .
@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:NP860459.RAmf3oNpEOx30P-JDxko_hugAOv7Zx0Ufa1eq9EXqK0HQ130_head
{
this:
np:hasAssertion
dgn-np:NP860459.RAmf3oNpEOx30P-JDxko_hugAOv7Zx0Ufa1eq9EXqK0HQ130_assertion
;
np:hasProvenance
dgn-np:NP860459.RAmf3oNpEOx30P-JDxko_hugAOv7Zx0Ufa1eq9EXqK0HQ130_provenance
;
np:hasPublicationInfo
dgn-np:NP860459.RAmf3oNpEOx30P-JDxko_hugAOv7Zx0Ufa1eq9EXqK0HQ130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP860459.RAmf3oNpEOx30P-JDxko_hugAOv7Zx0Ufa1eq9EXqK0HQ130_assertion
a
np:Assertion
.
dgn-np:NP860459.RAmf3oNpEOx30P-JDxko_hugAOv7Zx0Ufa1eq9EXqK0HQ130_provenance
a
np:Provenance
.
dgn-np:NP860459.RAmf3oNpEOx30P-JDxko_hugAOv7Zx0Ufa1eq9EXqK0HQ130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP860459.RAmf3oNpEOx30P-JDxko_hugAOv7Zx0Ufa1eq9EXqK0HQ130_assertion
{
miriam-gene:11136
a
ncit:C16612
.
lld:C0018609
a
ncit:C7057
.
dgn-gda:DGN8e752de6c6e034fea5b93362f53992e0
sio:SIO_000628
miriam-gene:11136
,
lld:C0018609
;
a
sio:SIO_001122
.
}
dgn-np:NP860459.RAmf3oNpEOx30P-JDxko_hugAOv7Zx0Ufa1eq9EXqK0HQ130_provenance
{
dgn-np:NP860459.RAmf3oNpEOx30P-JDxko_hugAOv7Zx0Ufa1eq9EXqK0HQ130_assertion
dcterms:description
"[We thus show that ACE2 is necessary for the expression of the Hartnup transporter in intestine and suggest that the differential functional association of mutant B(0)AT1 transporters with ACE2 and collectrin in intestine and kidney, respectively, participates in the phenotypic heterogeneity of human Hartnup disorder.]. 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:19185582
;
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:NP860459.RAmf3oNpEOx30P-JDxko_hugAOv7Zx0Ufa1eq9EXqK0HQ130_publicationInfo
{
this:
dcterms:created
"2015-08-25T14:46:22+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" .
}