@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP51070.RA2_HHZMR6Uf6U6dYqTrT1FpzN2B1YPYLuNtFkx_f25ho
> .
@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:NP51070.RA2_HHZMR6Uf6U6dYqTrT1FpzN2B1YPYLuNtFkx_f25ho130_head
{
this:
np:hasAssertion
dgn-np:NP51070.RA2_HHZMR6Uf6U6dYqTrT1FpzN2B1YPYLuNtFkx_f25ho130_assertion
;
np:hasProvenance
dgn-np:NP51070.RA2_HHZMR6Uf6U6dYqTrT1FpzN2B1YPYLuNtFkx_f25ho130_provenance
;
np:hasPublicationInfo
dgn-np:NP51070.RA2_HHZMR6Uf6U6dYqTrT1FpzN2B1YPYLuNtFkx_f25ho130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP51070.RA2_HHZMR6Uf6U6dYqTrT1FpzN2B1YPYLuNtFkx_f25ho130_assertion
a
np:Assertion
.
dgn-np:NP51070.RA2_HHZMR6Uf6U6dYqTrT1FpzN2B1YPYLuNtFkx_f25ho130_provenance
a
np:Provenance
.
dgn-np:NP51070.RA2_HHZMR6Uf6U6dYqTrT1FpzN2B1YPYLuNtFkx_f25ho130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP51070.RA2_HHZMR6Uf6U6dYqTrT1FpzN2B1YPYLuNtFkx_f25ho130_assertion
{
miriam-gene:6721
a
ncit:C16612
.
lld:C0020473
a
ncit:C7057
.
dgn-gda:DGN5c75998006a695126ab19ef4ee092d5e
sio:SIO_000628
miriam-gene:6721
,
lld:C0020473
;
a
sio:SIO_001122
.
}
dgn-np:NP51070.RA2_HHZMR6Uf6U6dYqTrT1FpzN2B1YPYLuNtFkx_f25ho130_provenance
{
dgn-np:NP51070.RA2_HHZMR6Uf6U6dYqTrT1FpzN2B1YPYLuNtFkx_f25ho130_assertion
dcterms:description
"[An intronic single nucleotide polymorphism in ABCA1 and the APOE epsilon3 allele are associated with reduced LDLc lowering by statins and identify individuals who may be resistant to maximal LDLc lowering by statins.]. 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:20031551
;
prov:wasDerivedFrom
dgn-void:gad-20130706
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:gad-20130706
pav:importedOn
"2013-07-06"^^
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:NP51070.RA2_HHZMR6Uf6U6dYqTrT1FpzN2B1YPYLuNtFkx_f25ho130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:23+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" .
}