@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP882061.RANy9RDZoc2WE0FtQjtn8tBq5Ts15gtLf3msZ2hAxQSCU
> .
@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:NP882061.RANy9RDZoc2WE0FtQjtn8tBq5Ts15gtLf3msZ2hAxQSCU130_head
{
this:
np:hasAssertion
dgn-np:NP882061.RANy9RDZoc2WE0FtQjtn8tBq5Ts15gtLf3msZ2hAxQSCU130_assertion
;
np:hasProvenance
dgn-np:NP882061.RANy9RDZoc2WE0FtQjtn8tBq5Ts15gtLf3msZ2hAxQSCU130_provenance
;
np:hasPublicationInfo
dgn-np:NP882061.RANy9RDZoc2WE0FtQjtn8tBq5Ts15gtLf3msZ2hAxQSCU130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP882061.RANy9RDZoc2WE0FtQjtn8tBq5Ts15gtLf3msZ2hAxQSCU130_assertion
a
np:Assertion
.
dgn-np:NP882061.RANy9RDZoc2WE0FtQjtn8tBq5Ts15gtLf3msZ2hAxQSCU130_provenance
a
np:Provenance
.
dgn-np:NP882061.RANy9RDZoc2WE0FtQjtn8tBq5Ts15gtLf3msZ2hAxQSCU130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP882061.RANy9RDZoc2WE0FtQjtn8tBq5Ts15gtLf3msZ2hAxQSCU130_assertion
{
miriam-gene:26154
a
ncit:C16612
.
lld:C0019247
a
ncit:C7057
.
dgn-gda:DGN3229e9147bdef2c0bde186068264bdb7
sio:SIO_000628
miriam-gene:26154
,
lld:C0019247
;
a
sio:SIO_001121
.
}
dgn-np:NP882061.RANy9RDZoc2WE0FtQjtn8tBq5Ts15gtLf3msZ2hAxQSCU130_provenance
{
dgn-np:NP882061.RANy9RDZoc2WE0FtQjtn8tBq5Ts15gtLf3msZ2hAxQSCU130_assertion
dcterms:description
"[This article describes ABCA12 as a causative molecule involved in defects in HI, summarizes the known genetic disorders caused by genetic defects in ABCA lipid transporters, and highlights the prospects of prenatal diagnosis and gene therapy for HI.]. 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:16847209
;
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:NP882061.RANy9RDZoc2WE0FtQjtn8tBq5Ts15gtLf3msZ2hAxQSCU130_publicationInfo
{
this:
dcterms:created
"2015-08-25T14:46:37+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" .
}