@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP278333.RALfMRY57Js2B8HrML6GELmJqUdZ3scmiYFdbr7lYbNnU
> .
@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:NP278333.RALfMRY57Js2B8HrML6GELmJqUdZ3scmiYFdbr7lYbNnU130_head
{
this:
np:hasAssertion
dgn-np:NP278333.RALfMRY57Js2B8HrML6GELmJqUdZ3scmiYFdbr7lYbNnU130_assertion
;
np:hasProvenance
dgn-np:NP278333.RALfMRY57Js2B8HrML6GELmJqUdZ3scmiYFdbr7lYbNnU130_provenance
;
np:hasPublicationInfo
dgn-np:NP278333.RALfMRY57Js2B8HrML6GELmJqUdZ3scmiYFdbr7lYbNnU130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP278333.RALfMRY57Js2B8HrML6GELmJqUdZ3scmiYFdbr7lYbNnU130_assertion
a
np:Assertion
.
dgn-np:NP278333.RALfMRY57Js2B8HrML6GELmJqUdZ3scmiYFdbr7lYbNnU130_provenance
a
np:Provenance
.
dgn-np:NP278333.RALfMRY57Js2B8HrML6GELmJqUdZ3scmiYFdbr7lYbNnU130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP278333.RALfMRY57Js2B8HrML6GELmJqUdZ3scmiYFdbr7lYbNnU130_assertion
{
miriam-gene:57393
a
ncit:C16612
.
lld:C0018609
a
ncit:C7057
.
dgn-gda:DGN0d2a35b798f277c5a94ac442c006df4f
sio:SIO_000628
miriam-gene:57393
,
lld:C0018609
;
a
sio:SIO_001121
.
}
dgn-np:NP278333.RALfMRY57Js2B8HrML6GELmJqUdZ3scmiYFdbr7lYbNnU130_provenance
{
dgn-np:NP278333.RALfMRY57Js2B8HrML6GELmJqUdZ3scmiYFdbr7lYbNnU130_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-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:NP278333.RALfMRY57Js2B8HrML6GELmJqUdZ3scmiYFdbr7lYbNnU130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:37+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" .
}