@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP518537.RAKBHQgHHU_0TYySVWruWbeQoix-gS-oiCovyr1J7KFH8
> .
@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:NP518537.RAKBHQgHHU_0TYySVWruWbeQoix-gS-oiCovyr1J7KFH8130_head
{
this:
np:hasAssertion
dgn-np:NP518537.RAKBHQgHHU_0TYySVWruWbeQoix-gS-oiCovyr1J7KFH8130_assertion
;
np:hasProvenance
dgn-np:NP518537.RAKBHQgHHU_0TYySVWruWbeQoix-gS-oiCovyr1J7KFH8130_provenance
;
np:hasPublicationInfo
dgn-np:NP518537.RAKBHQgHHU_0TYySVWruWbeQoix-gS-oiCovyr1J7KFH8130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP518537.RAKBHQgHHU_0TYySVWruWbeQoix-gS-oiCovyr1J7KFH8130_assertion
a
np:Assertion
.
dgn-np:NP518537.RAKBHQgHHU_0TYySVWruWbeQoix-gS-oiCovyr1J7KFH8130_provenance
a
np:Provenance
.
dgn-np:NP518537.RAKBHQgHHU_0TYySVWruWbeQoix-gS-oiCovyr1J7KFH8130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP518537.RAKBHQgHHU_0TYySVWruWbeQoix-gS-oiCovyr1J7KFH8130_assertion
{
miriam-gene:3077
a
ncit:C16612
.
lld:C0282193
a
ncit:C7057
.
dgn-gda:DGNff2b5d496e8a298aaa2f374b68d7c9c8
sio:SIO_000628
miriam-gene:3077
,
lld:C0282193
;
a
sio:SIO_001122
.
}
dgn-np:NP518537.RAKBHQgHHU_0TYySVWruWbeQoix-gS-oiCovyr1J7KFH8130_provenance
{
dgn-np:NP518537.RAKBHQgHHU_0TYySVWruWbeQoix-gS-oiCovyr1J7KFH8130_assertion
dcterms:description
"[Although most adult patients with hereditary iron overload are homozygous for the C282Y mutation of the HFE gene, an increasing number with hereditary iron storage have an HFE genotype not characteristic of the disease.]. 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:16234038
;
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:NP518537.RAKBHQgHHU_0TYySVWruWbeQoix-gS-oiCovyr1J7KFH8130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:45:40+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: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" .
}