@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP218613.RA82_f2DjV1Z4h4BNH227T00BKE74pDko6uJjYdzlPY70
> .
@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:NP218613.RA82_f2DjV1Z4h4BNH227T00BKE74pDko6uJjYdzlPY70130_head
{
this:
np:hasAssertion
dgn-np:NP218613.RA82_f2DjV1Z4h4BNH227T00BKE74pDko6uJjYdzlPY70130_assertion
;
np:hasProvenance
dgn-np:NP218613.RA82_f2DjV1Z4h4BNH227T00BKE74pDko6uJjYdzlPY70130_provenance
;
np:hasPublicationInfo
dgn-np:NP218613.RA82_f2DjV1Z4h4BNH227T00BKE74pDko6uJjYdzlPY70130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP218613.RA82_f2DjV1Z4h4BNH227T00BKE74pDko6uJjYdzlPY70130_assertion
a
np:Assertion
.
dgn-np:NP218613.RA82_f2DjV1Z4h4BNH227T00BKE74pDko6uJjYdzlPY70130_provenance
a
np:Provenance
.
dgn-np:NP218613.RA82_f2DjV1Z4h4BNH227T00BKE74pDko6uJjYdzlPY70130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP218613.RA82_f2DjV1Z4h4BNH227T00BKE74pDko6uJjYdzlPY70130_assertion
{
miriam-gene:19
a
ncit:C16612
.
lld:C2931838
a
ncit:C7057
.
dgn-gda:DGN5e29afe21e700514df8f73148f91a060
sio:SIO_000628
miriam-gene:19
,
lld:C2931838
;
a
sio:SIO_001121
.
}
dgn-np:NP218613.RA82_f2DjV1Z4h4BNH227T00BKE74pDko6uJjYdzlPY70130_provenance
{
dgn-np:NP218613.RA82_f2DjV1Z4h4BNH227T00BKE74pDko6uJjYdzlPY70130_assertion
dcterms:description
"[Direct sequencing of all coding regions and splice site junctions of other HDL candidate genes revealed no additional mutations, indicating that combined defective ABCA1 alleles may result in familial HDL deficiency.]. 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:12009425
;
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:NP218613.RA82_f2DjV1Z4h4BNH227T00BKE74pDko6uJjYdzlPY70130_publicationInfo
{
this:
dcterms:created
"2015-08-25T14:39:44+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" .
}