@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP811302.RAkGPPphzF8ga_WPCKxLJLpjwKRHU6C3_Kj-aaCaw26AI
> .
@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:NP811302.RAkGPPphzF8ga_WPCKxLJLpjwKRHU6C3_Kj-aaCaw26AI130_head
{
this:
np:hasAssertion
dgn-np:NP811302.RAkGPPphzF8ga_WPCKxLJLpjwKRHU6C3_Kj-aaCaw26AI130_assertion
;
np:hasProvenance
dgn-np:NP811302.RAkGPPphzF8ga_WPCKxLJLpjwKRHU6C3_Kj-aaCaw26AI130_provenance
;
np:hasPublicationInfo
dgn-np:NP811302.RAkGPPphzF8ga_WPCKxLJLpjwKRHU6C3_Kj-aaCaw26AI130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP811302.RAkGPPphzF8ga_WPCKxLJLpjwKRHU6C3_Kj-aaCaw26AI130_assertion
a
np:Assertion
.
dgn-np:NP811302.RAkGPPphzF8ga_WPCKxLJLpjwKRHU6C3_Kj-aaCaw26AI130_provenance
a
np:Provenance
.
dgn-np:NP811302.RAkGPPphzF8ga_WPCKxLJLpjwKRHU6C3_Kj-aaCaw26AI130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP811302.RAkGPPphzF8ga_WPCKxLJLpjwKRHU6C3_Kj-aaCaw26AI130_assertion
{
miriam-gene:6925
a
ncit:C16612
.
lld:C0020479
a
ncit:C7057
.
dgn-gda:DGN80e5715906e6cc9d42d0994b16f0737a
sio:SIO_000628
miriam-gene:6925
,
lld:C0020479
;
a
sio:SIO_001121
.
}
dgn-np:NP811302.RAkGPPphzF8ga_WPCKxLJLpjwKRHU6C3_Kj-aaCaw26AI130_provenance
{
dgn-np:NP811302.RAkGPPphzF8ga_WPCKxLJLpjwKRHU6C3_Kj-aaCaw26AI130_assertion
dcterms:description
"[Although valuable information has been gained concerning the mechanisms involved in type III hyperlipoproteinemia by the study of the disease, the clinical expression of this disorder is variable, ranging from hypocholesterolemia to marked hypercholesterolemia in subjects with the same molecular defect (E2/2).]. 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:3000263
;
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:NP811302.RAkGPPphzF8ga_WPCKxLJLpjwKRHU6C3_Kj-aaCaw26AI130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:17+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" .
}