@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP778891.RAhf-87RimvI4vIVxXJOai2jYduPId_AMtM-Cr-Sx_Igo
> .
@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:NP778891.RAhf-87RimvI4vIVxXJOai2jYduPId_AMtM-Cr-Sx_Igo130_head
{
this:
np:hasAssertion
dgn-np:NP778891.RAhf-87RimvI4vIVxXJOai2jYduPId_AMtM-Cr-Sx_Igo130_assertion
;
np:hasProvenance
dgn-np:NP778891.RAhf-87RimvI4vIVxXJOai2jYduPId_AMtM-Cr-Sx_Igo130_provenance
;
np:hasPublicationInfo
dgn-np:NP778891.RAhf-87RimvI4vIVxXJOai2jYduPId_AMtM-Cr-Sx_Igo130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP778891.RAhf-87RimvI4vIVxXJOai2jYduPId_AMtM-Cr-Sx_Igo130_assertion
a
np:Assertion
.
dgn-np:NP778891.RAhf-87RimvI4vIVxXJOai2jYduPId_AMtM-Cr-Sx_Igo130_provenance
a
np:Provenance
.
dgn-np:NP778891.RAhf-87RimvI4vIVxXJOai2jYduPId_AMtM-Cr-Sx_Igo130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP778891.RAhf-87RimvI4vIVxXJOai2jYduPId_AMtM-Cr-Sx_Igo130_assertion
{
miriam-gene:7036
a
ncit:C16612
.
lld:C0162566
a
ncit:C7057
.
dgn-gda:DGN1a9ca9ef7adcf61e48d6d7b7ea026643
sio:SIO_000628
miriam-gene:7036
,
lld:C0162566
;
a
sio:SIO_001121
.
}
dgn-np:NP778891.RAhf-87RimvI4vIVxXJOai2jYduPId_AMtM-Cr-Sx_Igo130_provenance
{
dgn-np:NP778891.RAhf-87RimvI4vIVxXJOai2jYduPId_AMtM-Cr-Sx_Igo130_assertion
dcterms:description
"[To determine the prevalence of the HFE gene mutations p.Cys282Tyr (C282Y), p.His63Asp (H63D) and p.Ser65Cys (S65C), the p.Tyr250X (Y250X) mutation of the TFR2 gene, and HCV infection in patients with PCT in the Czech population, and to make comparison of the iron status among the respective genotypes.]. 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:18565178
;
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:NP778891.RAhf-87RimvI4vIVxXJOai2jYduPId_AMtM-Cr-Sx_Igo130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:52+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" .
}