@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP73782.RAwEBW-5Uv-TQO4ZRfX2yeMVzskU-pc8LPekZtiG11RpU
> .
@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:NP73782.RAwEBW-5Uv-TQO4ZRfX2yeMVzskU-pc8LPekZtiG11RpU130_head
{
this:
np:hasAssertion
dgn-np:NP73782.RAwEBW-5Uv-TQO4ZRfX2yeMVzskU-pc8LPekZtiG11RpU130_assertion
;
np:hasProvenance
dgn-np:NP73782.RAwEBW-5Uv-TQO4ZRfX2yeMVzskU-pc8LPekZtiG11RpU130_provenance
;
np:hasPublicationInfo
dgn-np:NP73782.RAwEBW-5Uv-TQO4ZRfX2yeMVzskU-pc8LPekZtiG11RpU130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP73782.RAwEBW-5Uv-TQO4ZRfX2yeMVzskU-pc8LPekZtiG11RpU130_assertion
a
np:Assertion
.
dgn-np:NP73782.RAwEBW-5Uv-TQO4ZRfX2yeMVzskU-pc8LPekZtiG11RpU130_provenance
a
np:Provenance
.
dgn-np:NP73782.RAwEBW-5Uv-TQO4ZRfX2yeMVzskU-pc8LPekZtiG11RpU130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP73782.RAwEBW-5Uv-TQO4ZRfX2yeMVzskU-pc8LPekZtiG11RpU130_assertion
{
miriam-gene:3077
a
ncit:C16612
.
lld:C0002874
a
ncit:C7057
.
dgn-gda:DGNb9f67808e9943c4162878ef792db3536
sio:SIO_000628
miriam-gene:3077
,
lld:C0002874
;
a
sio:SIO_001122
.
}
dgn-np:NP73782.RAwEBW-5Uv-TQO4ZRfX2yeMVzskU-pc8LPekZtiG11RpU130_provenance
{
dgn-np:NP73782.RAwEBW-5Uv-TQO4ZRfX2yeMVzskU-pc8LPekZtiG11RpU130_assertion
dcterms:description
"[It seems that MDS and AA patients are susceptible to iron overload, in the diseases itself and the mutations of HFE gene are not the major factor for iron overload in the patients.]. 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:19731820
;
prov:wasDerivedFrom
dgn-void:gad-20130706
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:gad-20130706
pav:importedOn
"2013-07-06"^^
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:NP73782.RAwEBW-5Uv-TQO4ZRfX2yeMVzskU-pc8LPekZtiG11RpU130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:36+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" .
}