@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP857109.RAVRDRUakw3oVThtsBJIgV6WyMHMQMGzdFW461z6Jia2w
> .
@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:NP857109.RAVRDRUakw3oVThtsBJIgV6WyMHMQMGzdFW461z6Jia2w130_head
{
this:
np:hasAssertion
dgn-np:NP857109.RAVRDRUakw3oVThtsBJIgV6WyMHMQMGzdFW461z6Jia2w130_assertion
;
np:hasProvenance
dgn-np:NP857109.RAVRDRUakw3oVThtsBJIgV6WyMHMQMGzdFW461z6Jia2w130_provenance
;
np:hasPublicationInfo
dgn-np:NP857109.RAVRDRUakw3oVThtsBJIgV6WyMHMQMGzdFW461z6Jia2w130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP857109.RAVRDRUakw3oVThtsBJIgV6WyMHMQMGzdFW461z6Jia2w130_assertion
a
np:Assertion
.
dgn-np:NP857109.RAVRDRUakw3oVThtsBJIgV6WyMHMQMGzdFW461z6Jia2w130_provenance
a
np:Provenance
.
dgn-np:NP857109.RAVRDRUakw3oVThtsBJIgV6WyMHMQMGzdFW461z6Jia2w130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP857109.RAVRDRUakw3oVThtsBJIgV6WyMHMQMGzdFW461z6Jia2w130_assertion
{
miriam-gene:4700
a
ncit:C16612
.
lld:C0392514
a
ncit:C7057
.
dgn-gda:DGN09c511744df994959af800357f3f66c3
sio:SIO_000628
miriam-gene:4700
,
lld:C0392514
;
a
sio:SIO_001121
.
}
dgn-np:NP857109.RAVRDRUakw3oVThtsBJIgV6WyMHMQMGzdFW461z6Jia2w130_provenance
{
dgn-np:NP857109.RAVRDRUakw3oVThtsBJIgV6WyMHMQMGzdFW461z6Jia2w130_assertion
dcterms:description
"[We evaluated 99 patients on chronic hemodialysis estimating their serum ferritin (SF) levels, transfusion rate, and prevalence of HLA A3, B7 and B14 alleles, which are considered to be more frequent in idiopathic hemochromatosis.]. 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:3226455
;
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:NP857109.RAVRDRUakw3oVThtsBJIgV6WyMHMQMGzdFW461z6Jia2w130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:44+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" .
}