@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP10088.RAFMwv1eNABny-mKcjGm0KI6O5_5lnODZRS2KxQpYRBcs
> .
@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:NP10088.RAFMwv1eNABny-mKcjGm0KI6O5_5lnODZRS2KxQpYRBcs130_head
{
this:
np:hasAssertion
dgn-np:NP10088.RAFMwv1eNABny-mKcjGm0KI6O5_5lnODZRS2KxQpYRBcs130_assertion
;
np:hasProvenance
dgn-np:NP10088.RAFMwv1eNABny-mKcjGm0KI6O5_5lnODZRS2KxQpYRBcs130_provenance
;
np:hasPublicationInfo
dgn-np:NP10088.RAFMwv1eNABny-mKcjGm0KI6O5_5lnODZRS2KxQpYRBcs130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP10088.RAFMwv1eNABny-mKcjGm0KI6O5_5lnODZRS2KxQpYRBcs130_assertion
a
np:Assertion
.
dgn-np:NP10088.RAFMwv1eNABny-mKcjGm0KI6O5_5lnODZRS2KxQpYRBcs130_provenance
a
np:Provenance
.
dgn-np:NP10088.RAFMwv1eNABny-mKcjGm0KI6O5_5lnODZRS2KxQpYRBcs130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP10088.RAFMwv1eNABny-mKcjGm0KI6O5_5lnODZRS2KxQpYRBcs130_assertion
{
miriam-gene:654
a
ncit:C16612
.
lld:C0018995
a
ncit:C7057
.
dgn-gda:DGN46778dce8052120357e38b7fba0ff112
sio:SIO_000628
miriam-gene:654
,
lld:C0018995
;
a
sio:SIO_001121
.
}
dgn-np:NP10088.RAFMwv1eNABny-mKcjGm0KI6O5_5lnODZRS2KxQpYRBcs130_provenance
{
dgn-np:NP10088.RAFMwv1eNABny-mKcjGm0KI6O5_5lnODZRS2KxQpYRBcs130_assertion
dcterms:description
"[The iron burden in Bmp6 mutant mice is significantly greater than that in mice deficient in the gene associated with classical hemochromatosis (Hfe), suggesting that mutations in BMP6 might cause iron overload in humans with severe juvenile hemochromatosis for which the genetic basis has not yet been characterized.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ;
wi:evidence
dgn-void:source_evidence_curated
;
sio:SIO_000772
miriam-pubmed:19252488
;
prov:wasDerivedFrom
dgn-void:ctd_human-20130708
;
prov:wasGeneratedBy
eco:ECO_0000218
.
dgn-void:ctd_human-20130708
pav:importedOn
"2013-07-24"^^
xsd:date
.
dgn-void:source_evidence_curated
a
eco:ECO_0000205
;
rdfs:comment
"Gene-disease associations manually curated."@en ;
rdfs:label
"DisGeNET evidence - CURATED"@en .
}
dgn-np:NP10088.RAFMwv1eNABny-mKcjGm0KI6O5_5lnODZRS2KxQpYRBcs130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:02+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" .
}