@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP565037.RAnzsYeM8sdtls77iU_ULBBpgEfsmMWimDTD0cDkNeozc
> .
@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:NP565037.RAnzsYeM8sdtls77iU_ULBBpgEfsmMWimDTD0cDkNeozc130_head
{
this:
np:hasAssertion
dgn-np:NP565037.RAnzsYeM8sdtls77iU_ULBBpgEfsmMWimDTD0cDkNeozc130_assertion
;
np:hasProvenance
dgn-np:NP565037.RAnzsYeM8sdtls77iU_ULBBpgEfsmMWimDTD0cDkNeozc130_provenance
;
np:hasPublicationInfo
dgn-np:NP565037.RAnzsYeM8sdtls77iU_ULBBpgEfsmMWimDTD0cDkNeozc130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP565037.RAnzsYeM8sdtls77iU_ULBBpgEfsmMWimDTD0cDkNeozc130_assertion
a
np:Assertion
.
dgn-np:NP565037.RAnzsYeM8sdtls77iU_ULBBpgEfsmMWimDTD0cDkNeozc130_provenance
a
np:Provenance
.
dgn-np:NP565037.RAnzsYeM8sdtls77iU_ULBBpgEfsmMWimDTD0cDkNeozc130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP565037.RAnzsYeM8sdtls77iU_ULBBpgEfsmMWimDTD0cDkNeozc130_assertion
{
miriam-gene:7531
a
ncit:C16612
.
lld:C0026986
a
ncit:C7057
.
dgn-gda:DGN8f439e7b3ab94e79e780aae6e2360dd1
sio:SIO_000628
miriam-gene:7531
,
lld:C0026986
;
a
sio:SIO_001121
.
}
dgn-np:NP565037.RAnzsYeM8sdtls77iU_ULBBpgEfsmMWimDTD0cDkNeozc130_provenance
{
dgn-np:NP565037.RAnzsYeM8sdtls77iU_ULBBpgEfsmMWimDTD0cDkNeozc130_assertion
dcterms:description
"[In myelodysplastic syndromes with ring sideroblasts (MDS-RS), the iron deposited in the mitochondria of RS is present in the form of mitochondrial ferritin (FTMT), but it is unknown whether FTMT overexpression is the cause or the result of mitochondrial iron deposition.]. 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:23573868
;
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:NP565037.RAnzsYeM8sdtls77iU_ULBBpgEfsmMWimDTD0cDkNeozc130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:40+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" .
}