@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP618290.RAFJT16MVj9KIYSR2YkGzV0C1BI2m8kPIleVOVKf9IXNc
> .
@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:NP618290.RAFJT16MVj9KIYSR2YkGzV0C1BI2m8kPIleVOVKf9IXNc130_head
{
this:
np:hasAssertion
dgn-np:NP618290.RAFJT16MVj9KIYSR2YkGzV0C1BI2m8kPIleVOVKf9IXNc130_assertion
;
np:hasProvenance
dgn-np:NP618290.RAFJT16MVj9KIYSR2YkGzV0C1BI2m8kPIleVOVKf9IXNc130_provenance
;
np:hasPublicationInfo
dgn-np:NP618290.RAFJT16MVj9KIYSR2YkGzV0C1BI2m8kPIleVOVKf9IXNc130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP618290.RAFJT16MVj9KIYSR2YkGzV0C1BI2m8kPIleVOVKf9IXNc130_assertion
a
np:Assertion
.
dgn-np:NP618290.RAFJT16MVj9KIYSR2YkGzV0C1BI2m8kPIleVOVKf9IXNc130_provenance
a
np:Provenance
.
dgn-np:NP618290.RAFJT16MVj9KIYSR2YkGzV0C1BI2m8kPIleVOVKf9IXNc130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP618290.RAFJT16MVj9KIYSR2YkGzV0C1BI2m8kPIleVOVKf9IXNc130_assertion
{
miriam-gene:335
a
ncit:C16612
.
lld:C0020474
a
ncit:C7057
.
dgn-gda:DGNb64ebfd10fb6cde69a73410bbab846b0
sio:SIO_000628
miriam-gene:335
,
lld:C0020474
;
a
sio:SIO_001121
.
}
dgn-np:NP618290.RAFJT16MVj9KIYSR2YkGzV0C1BI2m8kPIleVOVKf9IXNc130_provenance
{
dgn-np:NP618290.RAFJT16MVj9KIYSR2YkGzV0C1BI2m8kPIleVOVKf9IXNc130_assertion
dcterms:description
"[By using chemical cleavage mismatch analysis and the single strand conformation polymorphism technique, DNA fragments of the apo CIII gene, including the 5' flanking region and all the exons, were screened for sequence changes underlying the observed association between familial combined hyperlipidaemia (FCHL) and the apo AI-CIII-AIV gene cluster in affected individuals from eight FCHL families.]. 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:7889654
;
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:NP618290.RAFJT16MVj9KIYSR2YkGzV0C1BI2m8kPIleVOVKf9IXNc130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:13+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" .
}