@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP504843.RAERhSzxlOzawQ2fkWl3pIyBrnNXMHtywgow7WdPGkBhw
> .
@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:NP504843.RAERhSzxlOzawQ2fkWl3pIyBrnNXMHtywgow7WdPGkBhw130_head
{
this:
np:hasAssertion
dgn-np:NP504843.RAERhSzxlOzawQ2fkWl3pIyBrnNXMHtywgow7WdPGkBhw130_assertion
;
np:hasProvenance
dgn-np:NP504843.RAERhSzxlOzawQ2fkWl3pIyBrnNXMHtywgow7WdPGkBhw130_provenance
;
np:hasPublicationInfo
dgn-np:NP504843.RAERhSzxlOzawQ2fkWl3pIyBrnNXMHtywgow7WdPGkBhw130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP504843.RAERhSzxlOzawQ2fkWl3pIyBrnNXMHtywgow7WdPGkBhw130_assertion
a
np:Assertion
.
dgn-np:NP504843.RAERhSzxlOzawQ2fkWl3pIyBrnNXMHtywgow7WdPGkBhw130_provenance
a
np:Provenance
.
dgn-np:NP504843.RAERhSzxlOzawQ2fkWl3pIyBrnNXMHtywgow7WdPGkBhw130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP504843.RAERhSzxlOzawQ2fkWl3pIyBrnNXMHtywgow7WdPGkBhw130_assertion
{
miriam-gene:3077
a
ncit:C16612
.
lld:C0002871
a
ncit:C7057
.
dgn-gda:DGN1018b4e2f615996d77b0144802b56605
sio:SIO_000628
miriam-gene:3077
,
lld:C0002871
;
a
sio:SIO_001121
.
}
dgn-np:NP504843.RAERhSzxlOzawQ2fkWl3pIyBrnNXMHtywgow7WdPGkBhw130_provenance
{
dgn-np:NP504843.RAERhSzxlOzawQ2fkWl3pIyBrnNXMHtywgow7WdPGkBhw130_assertion
dcterms:description
"[The data indicated that differences in the extent of iron overload were not mediated by co-inheritance of the C282Y mutation in the HFE gene but could largely be explained by differences in the severity of anaemia and ineffective erythropoiesis, and in the age of the patient.]. 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:10583252
;
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:NP504843.RAERhSzxlOzawQ2fkWl3pIyBrnNXMHtywgow7WdPGkBhw130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:01+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" .
}