@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP230173.RA8eWVkXWaeyBSlgjoCaB5uXzNQCI2YZdEhSJYYhTd2n0
> .
@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:NP230173.RA8eWVkXWaeyBSlgjoCaB5uXzNQCI2YZdEhSJYYhTd2n0130_head
{
this:
np:hasAssertion
dgn-np:NP230173.RA8eWVkXWaeyBSlgjoCaB5uXzNQCI2YZdEhSJYYhTd2n0130_assertion
;
np:hasProvenance
dgn-np:NP230173.RA8eWVkXWaeyBSlgjoCaB5uXzNQCI2YZdEhSJYYhTd2n0130_provenance
;
np:hasPublicationInfo
dgn-np:NP230173.RA8eWVkXWaeyBSlgjoCaB5uXzNQCI2YZdEhSJYYhTd2n0130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP230173.RA8eWVkXWaeyBSlgjoCaB5uXzNQCI2YZdEhSJYYhTd2n0130_assertion
a
np:Assertion
.
dgn-np:NP230173.RA8eWVkXWaeyBSlgjoCaB5uXzNQCI2YZdEhSJYYhTd2n0130_provenance
a
np:Provenance
.
dgn-np:NP230173.RA8eWVkXWaeyBSlgjoCaB5uXzNQCI2YZdEhSJYYhTd2n0130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP230173.RA8eWVkXWaeyBSlgjoCaB5uXzNQCI2YZdEhSJYYhTd2n0130_assertion
{
miriam-gene:3077
a
ncit:C16612
.
lld:C0162316
a
ncit:C7057
.
dgn-gda:DGN6b5bd217afa164ae74ee5449910f0ecc
sio:SIO_000628
miriam-gene:3077
,
lld:C0162316
;
a
sio:SIO_001121
.
}
dgn-np:NP230173.RA8eWVkXWaeyBSlgjoCaB5uXzNQCI2YZdEhSJYYhTd2n0130_provenance
{
dgn-np:NP230173.RA8eWVkXWaeyBSlgjoCaB5uXzNQCI2YZdEhSJYYhTd2n0130_assertion
dcterms:description
"[HFE mutations increase iron absorption in patients with haemochromatosis, and the mean transferrin saturations and ferritin levels are mildly increased in heterozygotes, suggesting that HFE mutations may protect against iron depletion and iron deficiency anaemia.]. 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:12614226
;
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:NP230173.RA8eWVkXWaeyBSlgjoCaB5uXzNQCI2YZdEhSJYYhTd2n0130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:09+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" .
}