@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP336925.RAPmrUTyeqyUrWKmZNZknAUIS-xVt-lV7uv39veqej0Cw
> .
@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:NP336925.RAPmrUTyeqyUrWKmZNZknAUIS-xVt-lV7uv39veqej0Cw130_head
{
this:
np:hasAssertion
dgn-np:NP336925.RAPmrUTyeqyUrWKmZNZknAUIS-xVt-lV7uv39veqej0Cw130_assertion
;
np:hasProvenance
dgn-np:NP336925.RAPmrUTyeqyUrWKmZNZknAUIS-xVt-lV7uv39veqej0Cw130_provenance
;
np:hasPublicationInfo
dgn-np:NP336925.RAPmrUTyeqyUrWKmZNZknAUIS-xVt-lV7uv39veqej0Cw130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP336925.RAPmrUTyeqyUrWKmZNZknAUIS-xVt-lV7uv39veqej0Cw130_assertion
a
np:Assertion
.
dgn-np:NP336925.RAPmrUTyeqyUrWKmZNZknAUIS-xVt-lV7uv39veqej0Cw130_provenance
a
np:Provenance
.
dgn-np:NP336925.RAPmrUTyeqyUrWKmZNZknAUIS-xVt-lV7uv39veqej0Cw130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP336925.RAPmrUTyeqyUrWKmZNZknAUIS-xVt-lV7uv39veqej0Cw130_assertion
{
miriam-gene:19
a
ncit:C16612
.
lld:C0039292
a
ncit:C7057
.
dgn-gda:DGN43f42d14ff6abc8c547a7fad900018a8
sio:SIO_000628
miriam-gene:19
,
lld:C0039292
;
a
sio:SIO_001121
.
}
dgn-np:NP336925.RAPmrUTyeqyUrWKmZNZknAUIS-xVt-lV7uv39veqej0Cw130_provenance
{
dgn-np:NP336925.RAPmrUTyeqyUrWKmZNZknAUIS-xVt-lV7uv39veqej0Cw130_assertion
dcterms:description
"[The identification of mutations in ABCA1 in patients with Tangier disease and familial HDL deficiency demonstrated that inadequate transport of phospholipid and cholesterol to the extracellular space results in the hypercatabolism of lipid-poor nascent HDL particles.]. 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:11714841
;
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:NP336925.RAPmrUTyeqyUrWKmZNZknAUIS-xVt-lV7uv39veqej0Cw130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:44:18+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" .
}