@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP336926.RAZsfOGKw9h_OlhLuYdhRuvfW8CYf6rHad1zePMIb1Rzc
> .
@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:NP336926.RAZsfOGKw9h_OlhLuYdhRuvfW8CYf6rHad1zePMIb1Rzc130_head
{
this:
np:hasAssertion
dgn-np:NP336926.RAZsfOGKw9h_OlhLuYdhRuvfW8CYf6rHad1zePMIb1Rzc130_assertion
;
np:hasProvenance
dgn-np:NP336926.RAZsfOGKw9h_OlhLuYdhRuvfW8CYf6rHad1zePMIb1Rzc130_provenance
;
np:hasPublicationInfo
dgn-np:NP336926.RAZsfOGKw9h_OlhLuYdhRuvfW8CYf6rHad1zePMIb1Rzc130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP336926.RAZsfOGKw9h_OlhLuYdhRuvfW8CYf6rHad1zePMIb1Rzc130_assertion
a
np:Assertion
.
dgn-np:NP336926.RAZsfOGKw9h_OlhLuYdhRuvfW8CYf6rHad1zePMIb1Rzc130_provenance
a
np:Provenance
.
dgn-np:NP336926.RAZsfOGKw9h_OlhLuYdhRuvfW8CYf6rHad1zePMIb1Rzc130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP336926.RAZsfOGKw9h_OlhLuYdhRuvfW8CYf6rHad1zePMIb1Rzc130_assertion
{
miriam-gene:19
a
ncit:C16612
.
lld:C2931838
a
ncit:C7057
.
dgn-gda:DGN4859c6ec3abafbad82ca640a82790bc7
sio:SIO_000628
miriam-gene:19
,
lld:C2931838
;
a
sio:SIO_001121
.
}
dgn-np:NP336926.RAZsfOGKw9h_OlhLuYdhRuvfW8CYf6rHad1zePMIb1Rzc130_provenance
{
dgn-np:NP336926.RAZsfOGKw9h_OlhLuYdhRuvfW8CYf6rHad1zePMIb1Rzc130_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:NP336926.RAZsfOGKw9h_OlhLuYdhRuvfW8CYf6rHad1zePMIb1Rzc130_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" .
}