@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP297372.RA8GOoKH85RmbnfH1zs2Ljf6kB59-LAaFqRG3MAyauHQc
> .
@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:NP297372.RA8GOoKH85RmbnfH1zs2Ljf6kB59-LAaFqRG3MAyauHQc130_head
{
this:
np:hasAssertion
dgn-np:NP297372.RA8GOoKH85RmbnfH1zs2Ljf6kB59-LAaFqRG3MAyauHQc130_assertion
;
np:hasProvenance
dgn-np:NP297372.RA8GOoKH85RmbnfH1zs2Ljf6kB59-LAaFqRG3MAyauHQc130_provenance
;
np:hasPublicationInfo
dgn-np:NP297372.RA8GOoKH85RmbnfH1zs2Ljf6kB59-LAaFqRG3MAyauHQc130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP297372.RA8GOoKH85RmbnfH1zs2Ljf6kB59-LAaFqRG3MAyauHQc130_assertion
a
np:Assertion
.
dgn-np:NP297372.RA8GOoKH85RmbnfH1zs2Ljf6kB59-LAaFqRG3MAyauHQc130_provenance
a
np:Provenance
.
dgn-np:NP297372.RA8GOoKH85RmbnfH1zs2Ljf6kB59-LAaFqRG3MAyauHQc130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP297372.RA8GOoKH85RmbnfH1zs2Ljf6kB59-LAaFqRG3MAyauHQc130_assertion
{
miriam-gene:3949
a
ncit:C16612
.
lld:C0154251
a
ncit:C7057
.
dgn-gda:DGN262967cc2e3f835abf30d58f28fa79af
sio:SIO_000628
miriam-gene:3949
,
lld:C0154251
;
a
sio:SIO_001121
.
}
dgn-np:NP297372.RA8GOoKH85RmbnfH1zs2Ljf6kB59-LAaFqRG3MAyauHQc130_provenance
{
dgn-np:NP297372.RA8GOoKH85RmbnfH1zs2Ljf6kB59-LAaFqRG3MAyauHQc130_assertion
dcterms:description
"[Although there is consensus that lipid variables, especially lipoprotein(a), are heritable and that elevated LDL cholesterol levels should be treated, there are no clear definitions of the common familial lipid disorders associated with premature CHD (lipoprotein(a) excess, FCH, familial dyslipidemia, familial hypoalphalipoproteinemia, familial hypercholesterolemia), nor do we have clear guidelines for the treatment of most of these disorders.]. 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:8283932
;
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:NP297372.RA8GOoKH85RmbnfH1zs2Ljf6kB59-LAaFqRG3MAyauHQc130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:49+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" .
}