@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP179756.RA4mn_N2X2_oC9-MtyOKECZUG_XtktHlPOvreEhxNxLpo
> .
@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:NP179756.RA4mn_N2X2_oC9-MtyOKECZUG_XtktHlPOvreEhxNxLpo130_head
{
this:
np:hasAssertion
dgn-np:NP179756.RA4mn_N2X2_oC9-MtyOKECZUG_XtktHlPOvreEhxNxLpo130_assertion
;
np:hasProvenance
dgn-np:NP179756.RA4mn_N2X2_oC9-MtyOKECZUG_XtktHlPOvreEhxNxLpo130_provenance
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np:hasPublicationInfo
dgn-np:NP179756.RA4mn_N2X2_oC9-MtyOKECZUG_XtktHlPOvreEhxNxLpo130_publicationInfo
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a
np:Nanopublication
.
dgn-np:NP179756.RA4mn_N2X2_oC9-MtyOKECZUG_XtktHlPOvreEhxNxLpo130_assertion
a
np:Assertion
.
dgn-np:NP179756.RA4mn_N2X2_oC9-MtyOKECZUG_XtktHlPOvreEhxNxLpo130_provenance
a
np:Provenance
.
dgn-np:NP179756.RA4mn_N2X2_oC9-MtyOKECZUG_XtktHlPOvreEhxNxLpo130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP179756.RA4mn_N2X2_oC9-MtyOKECZUG_XtktHlPOvreEhxNxLpo130_assertion
{
miriam-gene:4023
a
ncit:C16612
.
lld:C0948242
a
ncit:C7057
.
dgn-gda:DGN03db2e9d9c123c767389f8c882fdeb2d
sio:SIO_000628
miriam-gene:4023
,
lld:C0948242
;
a
sio:SIO_001121
.
}
dgn-np:NP179756.RA4mn_N2X2_oC9-MtyOKECZUG_XtktHlPOvreEhxNxLpo130_provenance
{
dgn-np:NP179756.RA4mn_N2X2_oC9-MtyOKECZUG_XtktHlPOvreEhxNxLpo130_assertion
dcterms:description
"[The lipoprotein lipase gene could exert an influence in these circumstances.To study the relationship of pattern B LDL and lipids with N291S polymorphism of lipoprotein lipase (LPL) in FCH patients.Lipid profile, apolipoproteins, diameter of LDL and N291S polymorphism were determined in 93 patients with FCH and 286 individuals from the general population.FCH patients with N291S polymorphism showed a lower mean diameter of LDL.]. 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:19335919
;
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:NP179756.RA4mn_N2X2_oC9-MtyOKECZUG_XtktHlPOvreEhxNxLpo130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:37+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
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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
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