@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP810356.RAfiBkpu0lZ-j2PfJN4_qz16vFw0grbJiZf3lo9GD5rmg
> .
@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#
> .
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{
this:
np:hasAssertion
dgn-np:NP810356.RAfiBkpu0lZ-j2PfJN4_qz16vFw0grbJiZf3lo9GD5rmg130_assertion
;
np:hasProvenance
dgn-np:NP810356.RAfiBkpu0lZ-j2PfJN4_qz16vFw0grbJiZf3lo9GD5rmg130_provenance
;
np:hasPublicationInfo
dgn-np:NP810356.RAfiBkpu0lZ-j2PfJN4_qz16vFw0grbJiZf3lo9GD5rmg130_publicationInfo
;
a
np:Nanopublication
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a
np:Assertion
.
dgn-np:NP810356.RAfiBkpu0lZ-j2PfJN4_qz16vFw0grbJiZf3lo9GD5rmg130_provenance
a
np:Provenance
.
dgn-np:NP810356.RAfiBkpu0lZ-j2PfJN4_qz16vFw0grbJiZf3lo9GD5rmg130_publicationInfo
a
np:PublicationInfo
.
}
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{
miriam-gene:10483
a
ncit:C16612
.
lld:C1306589
a
ncit:C7057
.
dgn-gda:DGN1d528adca41f597f569620a8c725dcdd
sio:SIO_000628
miriam-gene:10483
,
lld:C1306589
;
a
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.
}
dgn-np:NP810356.RAfiBkpu0lZ-j2PfJN4_qz16vFw0grbJiZf3lo9GD5rmg130_provenance
{
dgn-np:NP810356.RAfiBkpu0lZ-j2PfJN4_qz16vFw0grbJiZf3lo9GD5rmg130_assertion
dcterms:description
"[We investigated whether the soluble transferrin receptor (TfR) level was related to the degree of iron overload in 20 patients with thalassaemia intermedia, six patients with congenital dyserythropoietic anaemia type II (CDA II) and four patients with X-linked congenital sideroblastic anaemia (XLSA).]. 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:10468869
;
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:NP810356.RAfiBkpu0lZ-j2PfJN4_qz16vFw0grbJiZf3lo9GD5rmg130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:17+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
<
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> , <
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
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dgn-void:disgenetrdf
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"v2.1.0" .
}