@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP621800.RAEf7nb8LsXDt0CVsjx-XN28cdAX6i9Yavmv1qc1vXTGM
> .
@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:NP621800.RAEf7nb8LsXDt0CVsjx-XN28cdAX6i9Yavmv1qc1vXTGM130_head
{
this:
np:hasAssertion
dgn-np:NP621800.RAEf7nb8LsXDt0CVsjx-XN28cdAX6i9Yavmv1qc1vXTGM130_assertion
;
np:hasProvenance
dgn-np:NP621800.RAEf7nb8LsXDt0CVsjx-XN28cdAX6i9Yavmv1qc1vXTGM130_provenance
;
np:hasPublicationInfo
dgn-np:NP621800.RAEf7nb8LsXDt0CVsjx-XN28cdAX6i9Yavmv1qc1vXTGM130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP621800.RAEf7nb8LsXDt0CVsjx-XN28cdAX6i9Yavmv1qc1vXTGM130_assertion
a
np:Assertion
.
dgn-np:NP621800.RAEf7nb8LsXDt0CVsjx-XN28cdAX6i9Yavmv1qc1vXTGM130_provenance
a
np:Provenance
.
dgn-np:NP621800.RAEf7nb8LsXDt0CVsjx-XN28cdAX6i9Yavmv1qc1vXTGM130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP621800.RAEf7nb8LsXDt0CVsjx-XN28cdAX6i9Yavmv1qc1vXTGM130_assertion
{
miriam-gene:3030
a
ncit:C16612
.
lld:C1455728
a
ncit:C7057
.
dgn-gda:DGNb72bc413372f82fb08dba45d406acdad
sio:SIO_000628
miriam-gene:3030
,
lld:C1455728
;
a
sio:SIO_001121
.
}
dgn-np:NP621800.RAEf7nb8LsXDt0CVsjx-XN28cdAX6i9Yavmv1qc1vXTGM130_provenance
{
dgn-np:NP621800.RAEf7nb8LsXDt0CVsjx-XN28cdAX6i9Yavmv1qc1vXTGM130_assertion
dcterms:description
"[Although this study was limited to one proband and her relatives, our observations suggest that there might be diverse etiological factors in China contributing to AFLP other than the frequently reported mutation in the LCHAD, and the metabolic basis for AFLP may be more heterogeneous than previously believed.]. 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:18031367
;
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:NP621800.RAEf7nb8LsXDt0CVsjx-XN28cdAX6i9Yavmv1qc1vXTGM130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:15+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" .
}