@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP887096.RA1uKvF1R53jXvV70icpIczEyhGEWNX1JAcVunLJUSeQM
> .
@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:NP887096.RA1uKvF1R53jXvV70icpIczEyhGEWNX1JAcVunLJUSeQM130_head
{
this:
np:hasAssertion
dgn-np:NP887096.RA1uKvF1R53jXvV70icpIczEyhGEWNX1JAcVunLJUSeQM130_assertion
;
np:hasProvenance
dgn-np:NP887096.RA1uKvF1R53jXvV70icpIczEyhGEWNX1JAcVunLJUSeQM130_provenance
;
np:hasPublicationInfo
dgn-np:NP887096.RA1uKvF1R53jXvV70icpIczEyhGEWNX1JAcVunLJUSeQM130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP887096.RA1uKvF1R53jXvV70icpIczEyhGEWNX1JAcVunLJUSeQM130_assertion
a
np:Assertion
.
dgn-np:NP887096.RA1uKvF1R53jXvV70icpIczEyhGEWNX1JAcVunLJUSeQM130_provenance
a
np:Provenance
.
dgn-np:NP887096.RA1uKvF1R53jXvV70icpIczEyhGEWNX1JAcVunLJUSeQM130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP887096.RA1uKvF1R53jXvV70icpIczEyhGEWNX1JAcVunLJUSeQM130_assertion
{
miriam-gene:1374
a
ncit:C16612
.
lld:C0020615
a
ncit:C7057
.
dgn-gda:DGN53132b7b083f1170df57579745ab8b35
sio:SIO_000628
miriam-gene:1374
,
lld:C0020615
;
a
sio:SIO_001121
.
}
dgn-np:NP887096.RA1uKvF1R53jXvV70icpIczEyhGEWNX1JAcVunLJUSeQM130_provenance
{
dgn-np:NP887096.RA1uKvF1R53jXvV70icpIczEyhGEWNX1JAcVunLJUSeQM130_assertion
dcterms:description
"[Genetic deficiency of L-CPT I, which has been reported in 16 patients from 13 families, is characterized by episodes of hypoketotic hypoglycemia beginning in early childhood and is usually associated with fasting or illness.]. 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:11441142
;
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:NP887096.RA1uKvF1R53jXvV70icpIczEyhGEWNX1JAcVunLJUSeQM130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:41:04+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" .
}