@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP234920.RAsi3izhx-h-vJntBzcfqrh4NvP5Pu6gejYqEYHfscDio
> .
@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:NP234920.RAsi3izhx-h-vJntBzcfqrh4NvP5Pu6gejYqEYHfscDio130_head
{
this:
np:hasAssertion
dgn-np:NP234920.RAsi3izhx-h-vJntBzcfqrh4NvP5Pu6gejYqEYHfscDio130_assertion
;
np:hasProvenance
dgn-np:NP234920.RAsi3izhx-h-vJntBzcfqrh4NvP5Pu6gejYqEYHfscDio130_provenance
;
np:hasPublicationInfo
dgn-np:NP234920.RAsi3izhx-h-vJntBzcfqrh4NvP5Pu6gejYqEYHfscDio130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP234920.RAsi3izhx-h-vJntBzcfqrh4NvP5Pu6gejYqEYHfscDio130_assertion
a
np:Assertion
.
dgn-np:NP234920.RAsi3izhx-h-vJntBzcfqrh4NvP5Pu6gejYqEYHfscDio130_provenance
a
np:Provenance
.
dgn-np:NP234920.RAsi3izhx-h-vJntBzcfqrh4NvP5Pu6gejYqEYHfscDio130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP234920.RAsi3izhx-h-vJntBzcfqrh4NvP5Pu6gejYqEYHfscDio130_assertion
{
miriam-gene:224
a
ncit:C16612
.
lld:C0037231
a
ncit:C7057
.
dgn-gda:DGNf59bf1b3648bdcf1e04ad41a4cdc3762
sio:SIO_000628
miriam-gene:224
,
lld:C0037231
;
a
sio:SIO_001121
.
}
dgn-np:NP234920.RAsi3izhx-h-vJntBzcfqrh4NvP5Pu6gejYqEYHfscDio130_provenance
{
dgn-np:NP234920.RAsi3izhx-h-vJntBzcfqrh4NvP5Pu6gejYqEYHfscDio130_assertion
dcterms:description
"[Sjögren-Larsson syndrome (SLS) is an inherited neurocutaneous disorder caused by mutations in the ALDH3A2 gene that encodes fatty aldehyde dehydrogenase (FALDH), an enzyme that catalyzes the oxidation of fatty aldehyde to fatty acid.]. 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:16996289
;
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:NP234920.RAsi3izhx-h-vJntBzcfqrh4NvP5Pu6gejYqEYHfscDio130_publicationInfo
{
this:
dcterms:created
"2015-08-25T14:39:53+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" .
}