@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP835713.RAKs2M8nwcAYmN7ibMPalGIGhmTwhYl211_JUXqFQj1n0
> .
@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/v3.0.0/void/
> .
dgn-np:NP835713.RAKs2M8nwcAYmN7ibMPalGIGhmTwhYl211_JUXqFQj1n0130_head
{
this:
np:hasAssertion
dgn-np:NP835713.RAKs2M8nwcAYmN7ibMPalGIGhmTwhYl211_JUXqFQj1n0130_assertion
;
np:hasProvenance
dgn-np:NP835713.RAKs2M8nwcAYmN7ibMPalGIGhmTwhYl211_JUXqFQj1n0130_provenance
;
np:hasPublicationInfo
dgn-np:NP835713.RAKs2M8nwcAYmN7ibMPalGIGhmTwhYl211_JUXqFQj1n0130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP835713.RAKs2M8nwcAYmN7ibMPalGIGhmTwhYl211_JUXqFQj1n0130_assertion
a
np:Assertion
.
dgn-np:NP835713.RAKs2M8nwcAYmN7ibMPalGIGhmTwhYl211_JUXqFQj1n0130_provenance
a
np:Provenance
.
dgn-np:NP835713.RAKs2M8nwcAYmN7ibMPalGIGhmTwhYl211_JUXqFQj1n0130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP835713.RAKs2M8nwcAYmN7ibMPalGIGhmTwhYl211_JUXqFQj1n0130_assertion
{
miriam-gene:10058
a
ncit:C16612
.
lld:C0019247
a
ncit:C7057
.
dgn-gda:DGN2303c74dc3fb8a9a4771a432722bf3c9
sio:SIO_000628
miriam-gene:10058
,
lld:C0019247
;
a
sio:SIO_001121
.
}
dgn-np:NP835713.RAKs2M8nwcAYmN7ibMPalGIGhmTwhYl211_JUXqFQj1n0130_provenance
{
dgn-np:NP835713.RAKs2M8nwcAYmN7ibMPalGIGhmTwhYl211_JUXqFQj1n0130_assertion
dcterms:description
"[These landmark discoveries that identified mutant ABC cholesterol transporters as the underlying causes of these genetic disorders have paved the way for better understanding of the cellular cholesterol transport process and HDL biogenesis.]. 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:12359125
;
prov:wasDerivedFrom
dgn-void:befree-20150227
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-20150227
pav:importedOn
"2015-02-27"^^
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:NP835713.RAKs2M8nwcAYmN7ibMPalGIGhmTwhYl211_JUXqFQj1n0130_publicationInfo
{
this:
dcterms:created
"2015-08-25T14:46:07+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
"v3.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v3.0.0" .
}