@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP531908.RAAhMcI1kI_WWULQixJFRXRax-KrddoFcahd7yEeytBaY
> .
@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/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@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/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v4.0.0/void/
> .
dgn-np:NP531908.RAAhMcI1kI_WWULQixJFRXRax-KrddoFcahd7yEeytBaY130_head
{
this:
np:hasAssertion
dgn-np:NP531908.RAAhMcI1kI_WWULQixJFRXRax-KrddoFcahd7yEeytBaY130_assertion
;
np:hasProvenance
dgn-np:NP531908.RAAhMcI1kI_WWULQixJFRXRax-KrddoFcahd7yEeytBaY130_provenance
;
np:hasPublicationInfo
dgn-np:NP531908.RAAhMcI1kI_WWULQixJFRXRax-KrddoFcahd7yEeytBaY130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP531908.RAAhMcI1kI_WWULQixJFRXRax-KrddoFcahd7yEeytBaY130_assertion
a
np:Assertion
.
dgn-np:NP531908.RAAhMcI1kI_WWULQixJFRXRax-KrddoFcahd7yEeytBaY130_provenance
a
np:Provenance
.
dgn-np:NP531908.RAAhMcI1kI_WWULQixJFRXRax-KrddoFcahd7yEeytBaY130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP531908.RAAhMcI1kI_WWULQixJFRXRax-KrddoFcahd7yEeytBaY130_assertion
{
miriam-gene:1917
a
ncit:C16612
.
lld:C0020445
a
ncit:C7057
.
dgn-gda:DGN60e79d6ab187a8776c89d493dfba3869
sio:SIO_000628
miriam-gene:1917
,
lld:C0020445
;
a
sio:SIO_001121
.
}
dgn-np:NP531908.RAAhMcI1kI_WWULQixJFRXRax-KrddoFcahd7yEeytBaY130_provenance
{
dgn-np:NP531908.RAAhMcI1kI_WWULQixJFRXRax-KrddoFcahd7yEeytBaY130_assertion
dcterms:description
"[We have screened 38 unrelated hypocholesterolemic subjects as well as 25 unrelated familial hypercholesterolemia (FH) heterozygotes who responded particularly well to statin therapy for mutations in the 12 exons of the PCSK9 gene by DNA sequencing.]. 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:16424354
;
prov:wasDerivedFrom
dgn-void:befree-2016
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-2016
pav:importedOn
"2016-02-19"^^
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:NP531908.RAAhMcI1kI_WWULQixJFRXRax-KrddoFcahd7yEeytBaY130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:45:45+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:disgenetv3.0rdf
;
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
"v4.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v4.0.0" .
}