@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP775260.RAh_FWOUM1_oJVsF_6wsuLeKQXtX5bz_1Tnxerg8BGUZs
> .
@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/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@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/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v4.0.0/void/
> .
dgn-np:NP775260.RAh_FWOUM1_oJVsF_6wsuLeKQXtX5bz_1Tnxerg8BGUZs130_head
{
this:
np:hasAssertion
dgn-np:NP775260.RAh_FWOUM1_oJVsF_6wsuLeKQXtX5bz_1Tnxerg8BGUZs130_assertion
;
np:hasProvenance
dgn-np:NP775260.RAh_FWOUM1_oJVsF_6wsuLeKQXtX5bz_1Tnxerg8BGUZs130_provenance
;
np:hasPublicationInfo
dgn-np:NP775260.RAh_FWOUM1_oJVsF_6wsuLeKQXtX5bz_1Tnxerg8BGUZs130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP775260.RAh_FWOUM1_oJVsF_6wsuLeKQXtX5bz_1Tnxerg8BGUZs130_assertion
a
np:Assertion
.
dgn-np:NP775260.RAh_FWOUM1_oJVsF_6wsuLeKQXtX5bz_1Tnxerg8BGUZs130_provenance
a
np:Provenance
.
dgn-np:NP775260.RAh_FWOUM1_oJVsF_6wsuLeKQXtX5bz_1Tnxerg8BGUZs130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP775260.RAh_FWOUM1_oJVsF_6wsuLeKQXtX5bz_1Tnxerg8BGUZs130_assertion
{
miriam-gene:3077
a
ncit:C16612
.
lld:C0392514
a
ncit:C7057
.
dgn-gda:DGN5de344ae468dfe931fd975bb9fa6246b
sio:SIO_000628
miriam-gene:3077
,
lld:C0392514
;
a
sio:SIO_001122
.
}
dgn-np:NP775260.RAh_FWOUM1_oJVsF_6wsuLeKQXtX5bz_1Tnxerg8BGUZs130_provenance
{
dgn-np:NP775260.RAh_FWOUM1_oJVsF_6wsuLeKQXtX5bz_1Tnxerg8BGUZs130_assertion
dcterms:description
"[Most types of genetic hemochromatosis are due to mutations in the HFE gene, although similar iron overload and organ damage can also result from mutations in genes other than HFE in rare types of hemochromatosis.]. 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:19907151
;
prov:wasDerivedFrom
dgn-void:befree-2016
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-2016
pav:importedOn
"2016-02-19"^^
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:NP775260.RAh_FWOUM1_oJVsF_6wsuLeKQXtX5bz_1Tnxerg8BGUZs130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:47:36+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:disgenetv3.0rdf
;
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
"v4.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v4.0.0" .
}