@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP576221.RAMVgvVTyID7JD-L5LgFKWc0MKPZYDcqmkUmci6juEDPA
> .
@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:NP576221.RAMVgvVTyID7JD-L5LgFKWc0MKPZYDcqmkUmci6juEDPA130_head
{
this:
np:hasAssertion
dgn-np:NP576221.RAMVgvVTyID7JD-L5LgFKWc0MKPZYDcqmkUmci6juEDPA130_assertion
;
np:hasProvenance
dgn-np:NP576221.RAMVgvVTyID7JD-L5LgFKWc0MKPZYDcqmkUmci6juEDPA130_provenance
;
np:hasPublicationInfo
dgn-np:NP576221.RAMVgvVTyID7JD-L5LgFKWc0MKPZYDcqmkUmci6juEDPA130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP576221.RAMVgvVTyID7JD-L5LgFKWc0MKPZYDcqmkUmci6juEDPA130_assertion
a
np:Assertion
.
dgn-np:NP576221.RAMVgvVTyID7JD-L5LgFKWc0MKPZYDcqmkUmci6juEDPA130_provenance
a
np:Provenance
.
dgn-np:NP576221.RAMVgvVTyID7JD-L5LgFKWc0MKPZYDcqmkUmci6juEDPA130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP576221.RAMVgvVTyID7JD-L5LgFKWc0MKPZYDcqmkUmci6juEDPA130_assertion
{
miriam-gene:2177
a
ncit:C16612
.
lld:C0268596
a
ncit:C7057
.
dgn-gda:DGNd19258bd452fb92d6031ebf7c4a1807a
sio:SIO_000628
miriam-gene:2177
,
lld:C0268596
;
a
sio:SIO_001121
.
}
dgn-np:NP576221.RAMVgvVTyID7JD-L5LgFKWc0MKPZYDcqmkUmci6juEDPA130_provenance
{
dgn-np:NP576221.RAMVgvVTyID7JD-L5LgFKWc0MKPZYDcqmkUmci6juEDPA130_assertion
dcterms:description
"[Our results provide a structural and functional framework that could help to elucidate the role that an increased cellular FAD content obtained from riboflavin supplementation may play in the molecular pathogenesis of not only MADD, but genetic disorders of flavoproteins in general.]. 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:19088074
;
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:NP576221.RAMVgvVTyID7JD-L5LgFKWc0MKPZYDcqmkUmci6juEDPA130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:47+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" .
}