@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP786993.RASwRnHoK6jP9fXYKAVec2Bc3AKe31IgHG5buEbcmiN88
> .
@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:NP786993.RASwRnHoK6jP9fXYKAVec2Bc3AKe31IgHG5buEbcmiN88130_head
{
this:
np:hasAssertion
dgn-np:NP786993.RASwRnHoK6jP9fXYKAVec2Bc3AKe31IgHG5buEbcmiN88130_assertion
;
np:hasProvenance
dgn-np:NP786993.RASwRnHoK6jP9fXYKAVec2Bc3AKe31IgHG5buEbcmiN88130_provenance
;
np:hasPublicationInfo
dgn-np:NP786993.RASwRnHoK6jP9fXYKAVec2Bc3AKe31IgHG5buEbcmiN88130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP786993.RASwRnHoK6jP9fXYKAVec2Bc3AKe31IgHG5buEbcmiN88130_assertion
a
np:Assertion
.
dgn-np:NP786993.RASwRnHoK6jP9fXYKAVec2Bc3AKe31IgHG5buEbcmiN88130_provenance
a
np:Provenance
.
dgn-np:NP786993.RASwRnHoK6jP9fXYKAVec2Bc3AKe31IgHG5buEbcmiN88130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP786993.RASwRnHoK6jP9fXYKAVec2Bc3AKe31IgHG5buEbcmiN88130_assertion
{
miriam-gene:3949
a
ncit:C16612
.
lld:C0020445
a
ncit:C7057
.
dgn-gda:DGN2a3e0678a8d2340ce6f2578e2e1a0242
sio:SIO_000628
miriam-gene:3949
,
lld:C0020445
;
a
sio:SIO_001121
.
}
dgn-np:NP786993.RASwRnHoK6jP9fXYKAVec2Bc3AKe31IgHG5buEbcmiN88130_provenance
{
dgn-np:NP786993.RASwRnHoK6jP9fXYKAVec2Bc3AKe31IgHG5buEbcmiN88130_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-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:NP786993.RASwRnHoK6jP9fXYKAVec2Bc3AKe31IgHG5buEbcmiN88130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:47:41+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" .
}