@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP977608.RAzyy_-USEGTO8EddJa1Gp__Fu29xWOdPgfTByEAhlcaA
> .
@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:NP977608.RAzyy_-USEGTO8EddJa1Gp__Fu29xWOdPgfTByEAhlcaA130_head
{
this:
np:hasAssertion
dgn-np:NP977608.RAzyy_-USEGTO8EddJa1Gp__Fu29xWOdPgfTByEAhlcaA130_assertion
;
np:hasProvenance
dgn-np:NP977608.RAzyy_-USEGTO8EddJa1Gp__Fu29xWOdPgfTByEAhlcaA130_provenance
;
np:hasPublicationInfo
dgn-np:NP977608.RAzyy_-USEGTO8EddJa1Gp__Fu29xWOdPgfTByEAhlcaA130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP977608.RAzyy_-USEGTO8EddJa1Gp__Fu29xWOdPgfTByEAhlcaA130_assertion
a
np:Assertion
.
dgn-np:NP977608.RAzyy_-USEGTO8EddJa1Gp__Fu29xWOdPgfTByEAhlcaA130_provenance
a
np:Provenance
.
dgn-np:NP977608.RAzyy_-USEGTO8EddJa1Gp__Fu29xWOdPgfTByEAhlcaA130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP977608.RAzyy_-USEGTO8EddJa1Gp__Fu29xWOdPgfTByEAhlcaA130_assertion
{
miriam-gene:338
a
ncit:C16612
.
lld:C0745103
a
ncit:C7057
.
dgn-gda:DGN4700efff93b69aa4f07ce5d439936047
sio:SIO_000628
miriam-gene:338
,
lld:C0745103
;
a
sio:SIO_001121
.
}
dgn-np:NP977608.RAzyy_-USEGTO8EddJa1Gp__Fu29xWOdPgfTByEAhlcaA130_provenance
{
dgn-np:NP977608.RAzyy_-USEGTO8EddJa1Gp__Fu29xWOdPgfTByEAhlcaA130_assertion
dcterms:description
"[A large number of genetic markers, mostly single nucleotide polymorphisms (SNP) or mutations in three genes, implicated in autosomal dominant hypercholesterolemia (ADH), viz APOB (apolipoprotein B), LDLR (low density lipoprotein receptor) and PCSK9 (proprotein convertase subtilisin/kexin type-9), have been identified and characterized.]. 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:22534770
;
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:NP977608.RAzyy_-USEGTO8EddJa1Gp__Fu29xWOdPgfTByEAhlcaA130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:49:07+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" .
}