@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP277505.RASLpqPvVGUmD07XSMpe0NKYm_JPDf91J1cYRZVeFQ1zc
> .
@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:NP277505.RASLpqPvVGUmD07XSMpe0NKYm_JPDf91J1cYRZVeFQ1zc130_head
{
this:
np:hasAssertion
dgn-np:NP277505.RASLpqPvVGUmD07XSMpe0NKYm_JPDf91J1cYRZVeFQ1zc130_assertion
;
np:hasProvenance
dgn-np:NP277505.RASLpqPvVGUmD07XSMpe0NKYm_JPDf91J1cYRZVeFQ1zc130_provenance
;
np:hasPublicationInfo
dgn-np:NP277505.RASLpqPvVGUmD07XSMpe0NKYm_JPDf91J1cYRZVeFQ1zc130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP277505.RASLpqPvVGUmD07XSMpe0NKYm_JPDf91J1cYRZVeFQ1zc130_assertion
a
np:Assertion
.
dgn-np:NP277505.RASLpqPvVGUmD07XSMpe0NKYm_JPDf91J1cYRZVeFQ1zc130_provenance
a
np:Provenance
.
dgn-np:NP277505.RASLpqPvVGUmD07XSMpe0NKYm_JPDf91J1cYRZVeFQ1zc130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP277505.RASLpqPvVGUmD07XSMpe0NKYm_JPDf91J1cYRZVeFQ1zc130_assertion
{
miriam-gene:1917
a
ncit:C16612
.
lld:C0006826
a
ncit:C7057
.
dgn-gda:DGN98cefc001789999682724a17a31e3252
sio:SIO_000628
miriam-gene:1917
,
lld:C0006826
;
a
sio:SIO_001121
.
}
dgn-np:NP277505.RASLpqPvVGUmD07XSMpe0NKYm_JPDf91J1cYRZVeFQ1zc130_provenance
{
dgn-np:NP277505.RASLpqPvVGUmD07XSMpe0NKYm_JPDf91J1cYRZVeFQ1zc130_assertion
dcterms:description
"[We anticipate that these data may advance the development of personalized statin use for reducing the risk of cancer as well as cardiovascular disease among the approximately 25 million people currently using statins worldwide.]. 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:20403997
;
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:NP277505.RASLpqPvVGUmD07XSMpe0NKYm_JPDf91J1cYRZVeFQ1zc130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:36+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" .
}