@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP841812.RA9XV-GxvZ1s1_gnurDO4cdMZCCQN_P2pZTp0MUuSPgWw
> .
@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:NP841812.RA9XV-GxvZ1s1_gnurDO4cdMZCCQN_P2pZTp0MUuSPgWw130_head
{
this:
np:hasAssertion
dgn-np:NP841812.RA9XV-GxvZ1s1_gnurDO4cdMZCCQN_P2pZTp0MUuSPgWw130_assertion
;
np:hasProvenance
dgn-np:NP841812.RA9XV-GxvZ1s1_gnurDO4cdMZCCQN_P2pZTp0MUuSPgWw130_provenance
;
np:hasPublicationInfo
dgn-np:NP841812.RA9XV-GxvZ1s1_gnurDO4cdMZCCQN_P2pZTp0MUuSPgWw130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP841812.RA9XV-GxvZ1s1_gnurDO4cdMZCCQN_P2pZTp0MUuSPgWw130_assertion
a
np:Assertion
.
dgn-np:NP841812.RA9XV-GxvZ1s1_gnurDO4cdMZCCQN_P2pZTp0MUuSPgWw130_provenance
a
np:Provenance
.
dgn-np:NP841812.RA9XV-GxvZ1s1_gnurDO4cdMZCCQN_P2pZTp0MUuSPgWw130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP841812.RA9XV-GxvZ1s1_gnurDO4cdMZCCQN_P2pZTp0MUuSPgWw130_assertion
{
miriam-gene:255738
a
ncit:C16612
.
lld:C1704417
a
ncit:C7057
.
dgn-gda:DGN7054439e2c8e8a1535f9b398f5e1e984
sio:SIO_000628
miriam-gene:255738
,
lld:C1704417
;
a
sio:SIO_001121
.
}
dgn-np:NP841812.RA9XV-GxvZ1s1_gnurDO4cdMZCCQN_P2pZTp0MUuSPgWw130_provenance
{
dgn-np:NP841812.RA9XV-GxvZ1s1_gnurDO4cdMZCCQN_P2pZTp0MUuSPgWw130_assertion
dcterms:description
"[The aim of the present study was to investigate the relationship between circulating PCSK9 (proprotein convertase subtilisin kexin type 9) and FCHL (familial combined hyperlipidaemia) and, when positive, to determine the strength of its heritability.]. 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:21539517
;
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:NP841812.RA9XV-GxvZ1s1_gnurDO4cdMZCCQN_P2pZTp0MUuSPgWw130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:34+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" .
}