@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP86549.RA5MtMZqG3BUiQF5kjHCgfuRciykNZra4_96PRSzOOL4Y
> .
@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:NP86549.RA5MtMZqG3BUiQF5kjHCgfuRciykNZra4_96PRSzOOL4Y130_head
{
this:
np:hasAssertion
dgn-np:NP86549.RA5MtMZqG3BUiQF5kjHCgfuRciykNZra4_96PRSzOOL4Y130_assertion
;
np:hasProvenance
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np:hasPublicationInfo
dgn-np:NP86549.RA5MtMZqG3BUiQF5kjHCgfuRciykNZra4_96PRSzOOL4Y130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP86549.RA5MtMZqG3BUiQF5kjHCgfuRciykNZra4_96PRSzOOL4Y130_assertion
a
np:Assertion
.
dgn-np:NP86549.RA5MtMZqG3BUiQF5kjHCgfuRciykNZra4_96PRSzOOL4Y130_provenance
a
np:Provenance
.
dgn-np:NP86549.RA5MtMZqG3BUiQF5kjHCgfuRciykNZra4_96PRSzOOL4Y130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP86549.RA5MtMZqG3BUiQF5kjHCgfuRciykNZra4_96PRSzOOL4Y130_assertion
{
miriam-gene:3156
a
ncit:C16612
.
lld:C0242339
a
ncit:C7057
.
dgn-gda:DGNda8e63610a97168a11ea4936f4116855
sio:SIO_000628
miriam-gene:3156
,
lld:C0242339
;
a
sio:SIO_001122
.
}
dgn-np:NP86549.RA5MtMZqG3BUiQF5kjHCgfuRciykNZra4_96PRSzOOL4Y130_provenance
{
dgn-np:NP86549.RA5MtMZqG3BUiQF5kjHCgfuRciykNZra4_96PRSzOOL4Y130_assertion
dcterms:description
"[We have identified a common LDLR 3-UTR haplotype that is associated with attenuated lipid-lowering response to simvastatin treatment. Response was further reduced in individuals with both LDLR and previously described HMGCR haplotypes. Previously identified racial differences in statin efficacy were partially explained by the greater prevalence of these combined haplotypes in blacks.]. 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:20413733
;
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:NP86549.RA5MtMZqG3BUiQF5kjHCgfuRciykNZra4_96PRSzOOL4Y130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:42+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
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"v2.1.0" .
}