@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP220211.RA_VuB2hN_0ku6adcjbsOueEspNyvtsXDoCcKsgJv5ZuY
> .
@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:NP220211.RA_VuB2hN_0ku6adcjbsOueEspNyvtsXDoCcKsgJv5ZuY130_head
{
this:
np:hasAssertion
dgn-np:NP220211.RA_VuB2hN_0ku6adcjbsOueEspNyvtsXDoCcKsgJv5ZuY130_assertion
;
np:hasProvenance
dgn-np:NP220211.RA_VuB2hN_0ku6adcjbsOueEspNyvtsXDoCcKsgJv5ZuY130_provenance
;
np:hasPublicationInfo
dgn-np:NP220211.RA_VuB2hN_0ku6adcjbsOueEspNyvtsXDoCcKsgJv5ZuY130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP220211.RA_VuB2hN_0ku6adcjbsOueEspNyvtsXDoCcKsgJv5ZuY130_assertion
a
np:Assertion
.
dgn-np:NP220211.RA_VuB2hN_0ku6adcjbsOueEspNyvtsXDoCcKsgJv5ZuY130_provenance
a
np:Provenance
.
dgn-np:NP220211.RA_VuB2hN_0ku6adcjbsOueEspNyvtsXDoCcKsgJv5ZuY130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP220211.RA_VuB2hN_0ku6adcjbsOueEspNyvtsXDoCcKsgJv5ZuY130_assertion
{
miriam-gene:3077
a
ncit:C16612
.
lld:C0010054
a
ncit:C7057
.
dgn-gda:DGN6a284a4db876ed6aec03306e435bf676
sio:SIO_000628
miriam-gene:3077
,
lld:C0010054
;
a
sio:SIO_001121
.
}
dgn-np:NP220211.RA_VuB2hN_0ku6adcjbsOueEspNyvtsXDoCcKsgJv5ZuY130_provenance
{
dgn-np:NP220211.RA_VuB2hN_0ku6adcjbsOueEspNyvtsXDoCcKsgJv5ZuY130_assertion
dcterms:description
"[There were no significant associations between elevated transferrin saturation in either men or women, or between elevated serum ferritin levels or HFE mutations in women, and the prevalence of coronary heart disease.]. 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:12427496
;
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:NP220211.RA_VuB2hN_0ku6adcjbsOueEspNyvtsXDoCcKsgJv5ZuY130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:02+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" .
}