@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP446690.RAriacKwTjU_RZlRdKociRmpNz10iHFmCIgcgw-1Ru0QM
> .
@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/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@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/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v3.0.0/void/
> .
dgn-np:NP446690.RAriacKwTjU_RZlRdKociRmpNz10iHFmCIgcgw-1Ru0QM130_head
{
this:
np:hasAssertion
dgn-np:NP446690.RAriacKwTjU_RZlRdKociRmpNz10iHFmCIgcgw-1Ru0QM130_assertion
;
np:hasProvenance
dgn-np:NP446690.RAriacKwTjU_RZlRdKociRmpNz10iHFmCIgcgw-1Ru0QM130_provenance
;
np:hasPublicationInfo
dgn-np:NP446690.RAriacKwTjU_RZlRdKociRmpNz10iHFmCIgcgw-1Ru0QM130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP446690.RAriacKwTjU_RZlRdKociRmpNz10iHFmCIgcgw-1Ru0QM130_assertion
a
np:Assertion
.
dgn-np:NP446690.RAriacKwTjU_RZlRdKociRmpNz10iHFmCIgcgw-1Ru0QM130_provenance
a
np:Provenance
.
dgn-np:NP446690.RAriacKwTjU_RZlRdKociRmpNz10iHFmCIgcgw-1Ru0QM130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP446690.RAriacKwTjU_RZlRdKociRmpNz10iHFmCIgcgw-1Ru0QM130_assertion
{
miriam-gene:3077
a
ncit:C16612
.
lld:C0003850
a
ncit:C7057
.
dgn-gda:DGNcebf4248ffb2f8d3debaf839f48e1266
sio:SIO_000628
miriam-gene:3077
,
lld:C0003850
;
a
sio:SIO_001122
.
}
dgn-np:NP446690.RAriacKwTjU_RZlRdKociRmpNz10iHFmCIgcgw-1Ru0QM130_provenance
{
dgn-np:NP446690.RAriacKwTjU_RZlRdKociRmpNz10iHFmCIgcgw-1Ru0QM130_assertion
dcterms:description
"[The finding of a similar prevalence of Cys282Tyr and His63Asp mutations in the HFE gene among controls and patients with coronary atherothrombotic disease, indirectly questions the possibility of an association between hereditary hemochromatosis and atherosclerosis.]. 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:10719381
;
prov:wasDerivedFrom
dgn-void:befree-20150227
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-20150227
pav:importedOn
"2015-02-27"^^
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:NP446690.RAriacKwTjU_RZlRdKociRmpNz10iHFmCIgcgw-1Ru0QM130_publicationInfo
{
this:
dcterms:created
"2015-08-25T14:42:01+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:disgenetv3.0rdf
;
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
"v3.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v3.0.0" .
}