@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP443901.RA4LVoSLMt5cqsfXVO46_Q0D-7r8pzCqmTHjOmUMxjZNQ
> .
@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:NP443901.RA4LVoSLMt5cqsfXVO46_Q0D-7r8pzCqmTHjOmUMxjZNQ130_head
{
this:
np:hasAssertion
dgn-np:NP443901.RA4LVoSLMt5cqsfXVO46_Q0D-7r8pzCqmTHjOmUMxjZNQ130_assertion
;
np:hasProvenance
dgn-np:NP443901.RA4LVoSLMt5cqsfXVO46_Q0D-7r8pzCqmTHjOmUMxjZNQ130_provenance
;
np:hasPublicationInfo
dgn-np:NP443901.RA4LVoSLMt5cqsfXVO46_Q0D-7r8pzCqmTHjOmUMxjZNQ130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP443901.RA4LVoSLMt5cqsfXVO46_Q0D-7r8pzCqmTHjOmUMxjZNQ130_assertion
a
np:Assertion
.
dgn-np:NP443901.RA4LVoSLMt5cqsfXVO46_Q0D-7r8pzCqmTHjOmUMxjZNQ130_provenance
a
np:Provenance
.
dgn-np:NP443901.RA4LVoSLMt5cqsfXVO46_Q0D-7r8pzCqmTHjOmUMxjZNQ130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP443901.RA4LVoSLMt5cqsfXVO46_Q0D-7r8pzCqmTHjOmUMxjZNQ130_assertion
{
miriam-gene:116519
a
ncit:C16612
.
lld:C0020480
a
ncit:C7057
.
dgn-gda:DGN30beabd275f20d445c45de0e13fba089
sio:SIO_000628
miriam-gene:116519
,
lld:C0020480
;
a
sio:SIO_001121
.
}
dgn-np:NP443901.RA4LVoSLMt5cqsfXVO46_Q0D-7r8pzCqmTHjOmUMxjZNQ130_provenance
{
dgn-np:NP443901.RA4LVoSLMt5cqsfXVO46_Q0D-7r8pzCqmTHjOmUMxjZNQ130_assertion
dcterms:description
"[Several single nucleotide polymorphisms in the APOA5 gene are associated with increased TG levels in humans, and some nonsense mutations affecting protein structure predispose for familial hypertriglyceridemia and late onset chylomicronemia.]. 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:21831376
;
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:NP443901.RA4LVoSLMt5cqsfXVO46_Q0D-7r8pzCqmTHjOmUMxjZNQ130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:24+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" .
}