@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP66556.RA7jhDKuhCGx_j1tccKicNolEzAj8KDSO0yBDtS6dzNPg
> .
@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:NP66556.RA7jhDKuhCGx_j1tccKicNolEzAj8KDSO0yBDtS6dzNPg130_head
{
this:
np:hasAssertion
dgn-np:NP66556.RA7jhDKuhCGx_j1tccKicNolEzAj8KDSO0yBDtS6dzNPg130_assertion
;
np:hasProvenance
dgn-np:NP66556.RA7jhDKuhCGx_j1tccKicNolEzAj8KDSO0yBDtS6dzNPg130_provenance
;
np:hasPublicationInfo
dgn-np:NP66556.RA7jhDKuhCGx_j1tccKicNolEzAj8KDSO0yBDtS6dzNPg130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP66556.RA7jhDKuhCGx_j1tccKicNolEzAj8KDSO0yBDtS6dzNPg130_assertion
a
np:Assertion
.
dgn-np:NP66556.RA7jhDKuhCGx_j1tccKicNolEzAj8KDSO0yBDtS6dzNPg130_provenance
a
np:Provenance
.
dgn-np:NP66556.RA7jhDKuhCGx_j1tccKicNolEzAj8KDSO0yBDtS6dzNPg130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP66556.RA7jhDKuhCGx_j1tccKicNolEzAj8KDSO0yBDtS6dzNPg130_assertion
{
miriam-gene:30061
a
ncit:C16612
.
lld:C0282193
a
ncit:C7057
.
dgn-gda:DGN9bf857b8d83bebc6a32901a75d04ee0c
sio:SIO_000628
miriam-gene:30061
,
lld:C0282193
;
a
sio:SIO_001122
.
}
dgn-np:NP66556.RA7jhDKuhCGx_j1tccKicNolEzAj8KDSO0yBDtS6dzNPg130_provenance
{
dgn-np:NP66556.RA7jhDKuhCGx_j1tccKicNolEzAj8KDSO0yBDtS6dzNPg130_assertion
dcterms:description
"[The simultaneous detection of 18 known HFE, TFR2 and FPN1 mutations and sequencing of the HAMP gene were performed to rule out the possible existence of genetic modifier factors related with iron overload.]. 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:17042772
;
prov:wasDerivedFrom
dgn-void:gad-20130706
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:gad-20130706
pav:importedOn
"2013-07-06"^^
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:NP66556.RA7jhDKuhCGx_j1tccKicNolEzAj8KDSO0yBDtS6dzNPg130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:31+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" .
}