@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP250579.RABhc-nQApdS58ijL82mCBgszS8rZjDk3lN0Rt3ytNST8
> .
@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:NP250579.RABhc-nQApdS58ijL82mCBgszS8rZjDk3lN0Rt3ytNST8130_head
{
this:
np:hasAssertion
dgn-np:NP250579.RABhc-nQApdS58ijL82mCBgszS8rZjDk3lN0Rt3ytNST8130_assertion
;
np:hasProvenance
dgn-np:NP250579.RABhc-nQApdS58ijL82mCBgszS8rZjDk3lN0Rt3ytNST8130_provenance
;
np:hasPublicationInfo
dgn-np:NP250579.RABhc-nQApdS58ijL82mCBgszS8rZjDk3lN0Rt3ytNST8130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP250579.RABhc-nQApdS58ijL82mCBgszS8rZjDk3lN0Rt3ytNST8130_assertion
a
np:Assertion
.
dgn-np:NP250579.RABhc-nQApdS58ijL82mCBgszS8rZjDk3lN0Rt3ytNST8130_provenance
a
np:Provenance
.
dgn-np:NP250579.RABhc-nQApdS58ijL82mCBgszS8rZjDk3lN0Rt3ytNST8130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP250579.RABhc-nQApdS58ijL82mCBgszS8rZjDk3lN0Rt3ytNST8130_assertion
{
miriam-gene:116519
a
ncit:C16612
.
lld:C0020476
a
ncit:C7057
.
dgn-gda:DGNcf611872ddf0ad695b6700d6fd787775
sio:SIO_000628
miriam-gene:116519
,
lld:C0020476
;
a
sio:SIO_001121
.
}
dgn-np:NP250579.RABhc-nQApdS58ijL82mCBgszS8rZjDk3lN0Rt3ytNST8130_provenance
{
dgn-np:NP250579.RABhc-nQApdS58ijL82mCBgszS8rZjDk3lN0Rt3ytNST8130_assertion
dcterms:description
"[In addition, it became evident, that there are rare mutations of the APOA5 gene which can be associated with specific complex phenotypes and different types of hyperlipoproteinemia, which includes extremely high triglyceride levels with multiple organ pathology.]. 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:23150946
;
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:NP250579.RABhc-nQApdS58ijL82mCBgszS8rZjDk3lN0Rt3ytNST8130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:20+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" .
}