@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP210978.RAdc_TeOm5AoEiftZiBQe-WKD4z1Vu7UTKnF1QjEcYSAA
> .
@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:NP210978.RAdc_TeOm5AoEiftZiBQe-WKD4z1Vu7UTKnF1QjEcYSAA130_assertion
;
np:hasProvenance
dgn-np:NP210978.RAdc_TeOm5AoEiftZiBQe-WKD4z1Vu7UTKnF1QjEcYSAA130_provenance
;
np:hasPublicationInfo
dgn-np:NP210978.RAdc_TeOm5AoEiftZiBQe-WKD4z1Vu7UTKnF1QjEcYSAA130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP210978.RAdc_TeOm5AoEiftZiBQe-WKD4z1Vu7UTKnF1QjEcYSAA130_assertion
a
np:Assertion
.
dgn-np:NP210978.RAdc_TeOm5AoEiftZiBQe-WKD4z1Vu7UTKnF1QjEcYSAA130_provenance
a
np:Provenance
.
dgn-np:NP210978.RAdc_TeOm5AoEiftZiBQe-WKD4z1Vu7UTKnF1QjEcYSAA130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP210978.RAdc_TeOm5AoEiftZiBQe-WKD4z1Vu7UTKnF1QjEcYSAA130_assertion
{
miriam-gene:57817
a
ncit:C16612
.
lld:C0002871
a
ncit:C7057
.
dgn-gda:DGN03343245a27441dcabc9d66c753203b7
sio:SIO_000628
miriam-gene:57817
,
lld:C0002871
;
a
sio:SIO_001121
.
}
dgn-np:NP210978.RAdc_TeOm5AoEiftZiBQe-WKD4z1Vu7UTKnF1QjEcYSAA130_provenance
{
dgn-np:NP210978.RAdc_TeOm5AoEiftZiBQe-WKD4z1Vu7UTKnF1QjEcYSAA130_assertion
dcterms:description
"[Evaluation of the effect of TMPRSS6 genotype on clinical outcomes in prospective studies in CHD may be useful to predict the outcomes of hepcidin manipulation, and to guide treatment personalization by optimizing anemia management.]. 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:23433094
;
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:NP210978.RAdc_TeOm5AoEiftZiBQe-WKD4z1Vu7UTKnF1QjEcYSAA130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:56+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
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"v2.1.0" .
}