@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP574757.RAtV3S5GE2NL5DThvPLzzbKypQThtRVWwHdvH4yxrYg5U
> .
@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:NP574757.RAtV3S5GE2NL5DThvPLzzbKypQThtRVWwHdvH4yxrYg5U130_head
{
this:
np:hasAssertion
dgn-np:NP574757.RAtV3S5GE2NL5DThvPLzzbKypQThtRVWwHdvH4yxrYg5U130_assertion
;
np:hasProvenance
dgn-np:NP574757.RAtV3S5GE2NL5DThvPLzzbKypQThtRVWwHdvH4yxrYg5U130_provenance
;
np:hasPublicationInfo
dgn-np:NP574757.RAtV3S5GE2NL5DThvPLzzbKypQThtRVWwHdvH4yxrYg5U130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP574757.RAtV3S5GE2NL5DThvPLzzbKypQThtRVWwHdvH4yxrYg5U130_assertion
a
np:Assertion
.
dgn-np:NP574757.RAtV3S5GE2NL5DThvPLzzbKypQThtRVWwHdvH4yxrYg5U130_provenance
a
np:Provenance
.
dgn-np:NP574757.RAtV3S5GE2NL5DThvPLzzbKypQThtRVWwHdvH4yxrYg5U130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP574757.RAtV3S5GE2NL5DThvPLzzbKypQThtRVWwHdvH4yxrYg5U130_assertion
{
miriam-gene:3077
a
ncit:C16612
.
lld:C0524851
a
ncit:C7057
.
dgn-gda:DGNd847dcad4de562df3750f712d995016f
sio:SIO_000628
miriam-gene:3077
,
lld:C0524851
;
a
sio:SIO_001121
.
}
dgn-np:NP574757.RAtV3S5GE2NL5DThvPLzzbKypQThtRVWwHdvH4yxrYg5U130_provenance
{
dgn-np:NP574757.RAtV3S5GE2NL5DThvPLzzbKypQThtRVWwHdvH4yxrYg5U130_assertion
dcterms:description
"[At the cellular level, the HFE mutant protein resulting from the H63D HFE gene variant is associated with iron dyshomeostasis, increased oxidative stress, glutamate release, tau phosphorylation, and alteration in inflammatory response, each of which is under investigation as a contributing factor to neurodegenerative diseases.]. 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:21346098
;
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:NP574757.RAtV3S5GE2NL5DThvPLzzbKypQThtRVWwHdvH4yxrYg5U130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:46+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" .
}