@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP292145.RAQAGPJS8ZLW-js6au6HfK49v6ERkvAtnxIdRGPun2Sjg
> .
@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:NP292145.RAQAGPJS8ZLW-js6au6HfK49v6ERkvAtnxIdRGPun2Sjg130_head
{
this:
np:hasAssertion
dgn-np:NP292145.RAQAGPJS8ZLW-js6au6HfK49v6ERkvAtnxIdRGPun2Sjg130_assertion
;
np:hasProvenance
dgn-np:NP292145.RAQAGPJS8ZLW-js6au6HfK49v6ERkvAtnxIdRGPun2Sjg130_provenance
;
np:hasPublicationInfo
dgn-np:NP292145.RAQAGPJS8ZLW-js6au6HfK49v6ERkvAtnxIdRGPun2Sjg130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP292145.RAQAGPJS8ZLW-js6au6HfK49v6ERkvAtnxIdRGPun2Sjg130_assertion
a
np:Assertion
.
dgn-np:NP292145.RAQAGPJS8ZLW-js6au6HfK49v6ERkvAtnxIdRGPun2Sjg130_provenance
a
np:Provenance
.
dgn-np:NP292145.RAQAGPJS8ZLW-js6au6HfK49v6ERkvAtnxIdRGPun2Sjg130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP292145.RAQAGPJS8ZLW-js6au6HfK49v6ERkvAtnxIdRGPun2Sjg130_assertion
{
miriam-gene:3077
a
ncit:C16612
.
lld:C0010054
a
ncit:C7057
.
dgn-gda:DGN51e5ffe2c3b31471e24271817de4202b
sio:SIO_000628
miriam-gene:3077
,
lld:C0010054
;
a
sio:SIO_001121
.
}
dgn-np:NP292145.RAQAGPJS8ZLW-js6au6HfK49v6ERkvAtnxIdRGPun2Sjg130_provenance
{
dgn-np:NP292145.RAQAGPJS8ZLW-js6au6HfK49v6ERkvAtnxIdRGPun2Sjg130_assertion
dcterms:description
"[The identification of mutations in the haemochromatosis gene (HFE) (C282Y and H63D) provides the unique opportunity to test whether genetic variants that are associated with tissue iron accumulation may influence the risk of coronary 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:10854101
;
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:NP292145.RAQAGPJS8ZLW-js6au6HfK49v6ERkvAtnxIdRGPun2Sjg130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:46+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" .
}