@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP777432.RAr5XF1lY59Wr2qXvq6dxsurNr2e3S3KPp5LRLd9a4lGE
> .
@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:NP777432.RAr5XF1lY59Wr2qXvq6dxsurNr2e3S3KPp5LRLd9a4lGE130_head
{
this:
np:hasAssertion
dgn-np:NP777432.RAr5XF1lY59Wr2qXvq6dxsurNr2e3S3KPp5LRLd9a4lGE130_assertion
;
np:hasProvenance
dgn-np:NP777432.RAr5XF1lY59Wr2qXvq6dxsurNr2e3S3KPp5LRLd9a4lGE130_provenance
;
np:hasPublicationInfo
dgn-np:NP777432.RAr5XF1lY59Wr2qXvq6dxsurNr2e3S3KPp5LRLd9a4lGE130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP777432.RAr5XF1lY59Wr2qXvq6dxsurNr2e3S3KPp5LRLd9a4lGE130_assertion
a
np:Assertion
.
dgn-np:NP777432.RAr5XF1lY59Wr2qXvq6dxsurNr2e3S3KPp5LRLd9a4lGE130_provenance
a
np:Provenance
.
dgn-np:NP777432.RAr5XF1lY59Wr2qXvq6dxsurNr2e3S3KPp5LRLd9a4lGE130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP777432.RAr5XF1lY59Wr2qXvq6dxsurNr2e3S3KPp5LRLd9a4lGE130_assertion
{
miriam-gene:6518
a
ncit:C16612
.
lld:C0024523
a
ncit:C7057
.
dgn-gda:DGN4fb3fc3b938afb5e1b1c47fed6cfe5a7
sio:SIO_000628
miriam-gene:6518
,
lld:C0024523
;
a
sio:SIO_001121
.
}
dgn-np:NP777432.RAr5XF1lY59Wr2qXvq6dxsurNr2e3S3KPp5LRLd9a4lGE130_provenance
{
dgn-np:NP777432.RAr5XF1lY59Wr2qXvq6dxsurNr2e3S3KPp5LRLd9a4lGE130_assertion
dcterms:description
"[GLUT5 expression seems extremely low in neonatal intestines, and limited absorptive capacities for fructose may explain the high incidence of malabsorption in infants and cause problems in adults unable to upregulate GLUT5 levels to match fructose concentrations in the diet.]. 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:23129794
;
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:NP777432.RAr5XF1lY59Wr2qXvq6dxsurNr2e3S3KPp5LRLd9a4lGE130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:51+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" .
}