@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP222397.RAO19kFHnROFJYTvoQmk0JGHPD9maHsgACUKNsO6DXgmU
> .
@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:NP222397.RAO19kFHnROFJYTvoQmk0JGHPD9maHsgACUKNsO6DXgmU130_head
{
this:
np:hasAssertion
dgn-np:NP222397.RAO19kFHnROFJYTvoQmk0JGHPD9maHsgACUKNsO6DXgmU130_assertion
;
np:hasProvenance
dgn-np:NP222397.RAO19kFHnROFJYTvoQmk0JGHPD9maHsgACUKNsO6DXgmU130_provenance
;
np:hasPublicationInfo
dgn-np:NP222397.RAO19kFHnROFJYTvoQmk0JGHPD9maHsgACUKNsO6DXgmU130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP222397.RAO19kFHnROFJYTvoQmk0JGHPD9maHsgACUKNsO6DXgmU130_assertion
a
np:Assertion
.
dgn-np:NP222397.RAO19kFHnROFJYTvoQmk0JGHPD9maHsgACUKNsO6DXgmU130_provenance
a
np:Provenance
.
dgn-np:NP222397.RAO19kFHnROFJYTvoQmk0JGHPD9maHsgACUKNsO6DXgmU130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP222397.RAO19kFHnROFJYTvoQmk0JGHPD9maHsgACUKNsO6DXgmU130_assertion
{
miriam-gene:3949
a
ncit:C16612
.
lld:C0242339
a
ncit:C7057
.
dgn-gda:DGNab8754c7181c82a90c1db2b4ae699b04
sio:SIO_000628
miriam-gene:3949
,
lld:C0242339
;
a
sio:SIO_001121
.
}
dgn-np:NP222397.RAO19kFHnROFJYTvoQmk0JGHPD9maHsgACUKNsO6DXgmU130_provenance
{
dgn-np:NP222397.RAO19kFHnROFJYTvoQmk0JGHPD9maHsgACUKNsO6DXgmU130_assertion
dcterms:description
"[Common familial lipid disorders associated with premature heart disease include familial lipoprotein(a) excess, familial dyslipidemia (elevated triglycerides and decreased HDL cholesterol), familial combined hyperlipidemia (elevations of LDL cholesterol and triglycerides, and often decreased HDL cholesterol), familial hypoapobetalipoproteinemia (elevated apolipoprotein B levels), familial hypoalphalipoproteinemia (low HDL cholesterol levels), and familial hypercholesterolemia (elevated LDL cholesterol levels).]. 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:7802728
;
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:NP222397.RAO19kFHnROFJYTvoQmk0JGHPD9maHsgACUKNsO6DXgmU130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:03+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" .
}