@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP649716.RA9eROUOo_2yg0yv8c91XM5UPQ_BulgBM9jkL6d_qrhXk
> .
@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/eco.owl#
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/2.0/
> .
@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/nanopublications.trig#
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/gene-disease-association.ttl#
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v2.1.0/void.ttl#
> .
dgn-np:NP649716.RA9eROUOo_2yg0yv8c91XM5UPQ_BulgBM9jkL6d_qrhXk130_head
{
this:
np:hasAssertion
dgn-np:NP649716.RA9eROUOo_2yg0yv8c91XM5UPQ_BulgBM9jkL6d_qrhXk130_assertion
;
np:hasProvenance
dgn-np:NP649716.RA9eROUOo_2yg0yv8c91XM5UPQ_BulgBM9jkL6d_qrhXk130_provenance
;
np:hasPublicationInfo
dgn-np:NP649716.RA9eROUOo_2yg0yv8c91XM5UPQ_BulgBM9jkL6d_qrhXk130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP649716.RA9eROUOo_2yg0yv8c91XM5UPQ_BulgBM9jkL6d_qrhXk130_assertion
a
np:Assertion
.
dgn-np:NP649716.RA9eROUOo_2yg0yv8c91XM5UPQ_BulgBM9jkL6d_qrhXk130_provenance
a
np:Provenance
.
dgn-np:NP649716.RA9eROUOo_2yg0yv8c91XM5UPQ_BulgBM9jkL6d_qrhXk130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP649716.RA9eROUOo_2yg0yv8c91XM5UPQ_BulgBM9jkL6d_qrhXk130_assertion
{
miriam-gene:23600
a
ncit:C16612
.
lld:C3280428
a
ncit:C7057
.
dgn-gda:DGNfe133aa4923044857f6a47abefbeb459
sio:SIO_000628
miriam-gene:23600
,
lld:C3280428
;
a
sio:SIO_001121
.
}
dgn-np:NP649716.RA9eROUOo_2yg0yv8c91XM5UPQ_BulgBM9jkL6d_qrhXk130_provenance
{
dgn-np:NP649716.RA9eROUOo_2yg0yv8c91XM5UPQ_BulgBM9jkL6d_qrhXk130_assertion
dcterms:description
"[Investigation of these pathways and the diseases associated with mutations in enzymes involved in the degradation of phytanic acid have led to the clarification of the pathophysiology of Refsum's disease, rhizomelic chondrodysplasia and AMACR (alpha-methylacyl-CoA racemase) 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:17956237
;
prov:wasDerivedFrom
dgn-void:befree-20140225
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-20140225
pav:importedOn
"2014-02-25"^^
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:NP649716.RA9eROUOo_2yg0yv8c91XM5UPQ_BulgBM9jkL6d_qrhXk130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:31+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:disgenetrdf
;
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
"v2.1.0.0" .
dgn-void:disgenetrdf
pav:version
"v2.1.0" .
}