@prefix dct: <
http://purl.org/dc/terms/
> .
@prefix orcid: <
http://orcid.org/
> .
@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP48486.RAmlyn1eMbEZMC_ptEpXKbx8fePApF0X5VvzilCt3k89Q
> .
@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 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:NP48486.RAmlyn1eMbEZMC_ptEpXKbx8fePApF0X5VvzilCt3k89Q130_head
{
this:
np:hasAssertion
dgn-np:NP48486.RAmlyn1eMbEZMC_ptEpXKbx8fePApF0X5VvzilCt3k89Q130_assertion
;
np:hasProvenance
dgn-np:NP48486.RAmlyn1eMbEZMC_ptEpXKbx8fePApF0X5VvzilCt3k89Q130_provenance
;
np:hasPublicationInfo
dgn-np:NP48486.RAmlyn1eMbEZMC_ptEpXKbx8fePApF0X5VvzilCt3k89Q130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP48486.RAmlyn1eMbEZMC_ptEpXKbx8fePApF0X5VvzilCt3k89Q130_assertion
a
np:Assertion
.
dgn-np:NP48486.RAmlyn1eMbEZMC_ptEpXKbx8fePApF0X5VvzilCt3k89Q130_provenance
a
np:Provenance
.
dgn-np:NP48486.RAmlyn1eMbEZMC_ptEpXKbx8fePApF0X5VvzilCt3k89Q130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP48486.RAmlyn1eMbEZMC_ptEpXKbx8fePApF0X5VvzilCt3k89Q130_assertion
{
miriam-gene:335
a
ncit:C16612
.
lld:C0020473
a
ncit:C7057
.
dgn-gda:DGN9bff01dc9c22c3edb8908035b711304a
sio:SIO_000628
miriam-gene:335
,
lld:C0020473
;
a
sio:SIO_001122
.
}
dgn-np:NP48486.RAmlyn1eMbEZMC_ptEpXKbx8fePApF0X5VvzilCt3k89Q130_provenance
{
dgn-np:NP48486.RAmlyn1eMbEZMC_ptEpXKbx8fePApF0X5VvzilCt3k89Q130_assertion
dct: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:NP48486.RAmlyn1eMbEZMC_ptEpXKbx8fePApF0X5VvzilCt3k89Q130_publicationInfo
{
this:
dct:created
"2014-10-02T12:32:22+02:00"^^
xsd:dateTime
;
dct:rights
<
http://opendatacommons.org/licenses/odbl/1.0/
> ;
dct:rightsHolder
dgn-void:IBIGroup
;
dct:subject
sio:SIO_000983
;
prv:usedData
dgn-void:disgenetrdf
;
pav:authoredBy
orcid:0000-0001-5999-6269
,
orcid:0000-0002-7534-7661
,
orcid:0000-0002-9383-528X
,
orcid:0000-0003-0169-8159
,
orcid:0000-0003-1244-7654
;
pav:createdBy
orcid:0000-0003-0169-8159
;
pav:version
"v2.1.0.0" .
dgn-void:disgenetrdf
pav:version
"v2.1.0" .
}