@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP50051.RAtTkOVpmNWLctd9ryS2rreeevXXVLhc8sDpVgB_QD9bE
> .
@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:NP50051.RAtTkOVpmNWLctd9ryS2rreeevXXVLhc8sDpVgB_QD9bE130_head
{
this:
np:hasAssertion
dgn-np:NP50051.RAtTkOVpmNWLctd9ryS2rreeevXXVLhc8sDpVgB_QD9bE130_assertion
;
np:hasProvenance
dgn-np:NP50051.RAtTkOVpmNWLctd9ryS2rreeevXXVLhc8sDpVgB_QD9bE130_provenance
;
np:hasPublicationInfo
dgn-np:NP50051.RAtTkOVpmNWLctd9ryS2rreeevXXVLhc8sDpVgB_QD9bE130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP50051.RAtTkOVpmNWLctd9ryS2rreeevXXVLhc8sDpVgB_QD9bE130_assertion
a
np:Assertion
.
dgn-np:NP50051.RAtTkOVpmNWLctd9ryS2rreeevXXVLhc8sDpVgB_QD9bE130_provenance
a
np:Provenance
.
dgn-np:NP50051.RAtTkOVpmNWLctd9ryS2rreeevXXVLhc8sDpVgB_QD9bE130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP50051.RAtTkOVpmNWLctd9ryS2rreeevXXVLhc8sDpVgB_QD9bE130_assertion
{
miriam-gene:148738
a
ncit:C16612
.
lld:C0011860
a
ncit:C7057
.
dgn-gda:DGN2104f3f79bedd950958c382416d4cdf7
sio:SIO_000628
miriam-gene:148738
,
lld:C0011860
;
a
sio:SIO_001122
.
}
dgn-np:NP50051.RAtTkOVpmNWLctd9ryS2rreeevXXVLhc8sDpVgB_QD9bE130_provenance
{
dgn-np:NP50051.RAtTkOVpmNWLctd9ryS2rreeevXXVLhc8sDpVgB_QD9bE130_assertion
dcterms:description
"[ HJV I222N and G320V are probably uncommon causes or modifiers of primary iron overload in adult whites and African Americans in Alabama. Double heterozygosity for HJV I222N and HFE C282Y may not promote increased iron absorption.]. 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:15610558
;
prov:wasDerivedFrom
dgn-void:gad-20150221
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:gad-20150221
pav:importedOn
"2015-02-21"^^
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:NP50051.RAtTkOVpmNWLctd9ryS2rreeevXXVLhc8sDpVgB_QD9bE130_publicationInfo
{
this:
dcterms:created
"2015-08-25T14:38:07+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" .
}