@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP650133.RA-skjfHsCUTPrMmKp8G67Eo-kA-IXHp3aQ-tayWpd1LM
> .
@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:NP650133.RA-skjfHsCUTPrMmKp8G67Eo-kA-IXHp3aQ-tayWpd1LM130_head
{
this:
np:hasAssertion
dgn-np:NP650133.RA-skjfHsCUTPrMmKp8G67Eo-kA-IXHp3aQ-tayWpd1LM130_assertion
;
np:hasProvenance
dgn-np:NP650133.RA-skjfHsCUTPrMmKp8G67Eo-kA-IXHp3aQ-tayWpd1LM130_provenance
;
np:hasPublicationInfo
dgn-np:NP650133.RA-skjfHsCUTPrMmKp8G67Eo-kA-IXHp3aQ-tayWpd1LM130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP650133.RA-skjfHsCUTPrMmKp8G67Eo-kA-IXHp3aQ-tayWpd1LM130_assertion
a
np:Assertion
.
dgn-np:NP650133.RA-skjfHsCUTPrMmKp8G67Eo-kA-IXHp3aQ-tayWpd1LM130_provenance
a
np:Provenance
.
dgn-np:NP650133.RA-skjfHsCUTPrMmKp8G67Eo-kA-IXHp3aQ-tayWpd1LM130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP650133.RA-skjfHsCUTPrMmKp8G67Eo-kA-IXHp3aQ-tayWpd1LM130_assertion
{
miriam-gene:26119
a
ncit:C16612
.
lld:C0020445
a
ncit:C7057
.
dgn-gda:DGN885ac07019b8e8a665cd7f1200df8976
sio:SIO_000628
miriam-gene:26119
,
lld:C0020445
;
a
sio:SIO_001121
.
}
dgn-np:NP650133.RA-skjfHsCUTPrMmKp8G67Eo-kA-IXHp3aQ-tayWpd1LM130_provenance
{
dgn-np:NP650133.RA-skjfHsCUTPrMmKp8G67Eo-kA-IXHp3aQ-tayWpd1LM130_assertion
dcterms:description
"[More recently, defects in two other genes, LDLRAP1 and PCSK9, have been found in patients with FH and investigation of these has shed new light on the functioning and complexity of the LDL receptor pathway.]. 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:20073037
;
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:NP650133.RA-skjfHsCUTPrMmKp8G67Eo-kA-IXHp3aQ-tayWpd1LM130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:32+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" .
}