@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP446943.RAu_Dl4EH71VLyeRZJaNtKwiQvLz8PBKd5aGEKTloYakQ
> .
@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:NP446943.RAu_Dl4EH71VLyeRZJaNtKwiQvLz8PBKd5aGEKTloYakQ130_head
{
this:
np:hasAssertion
dgn-np:NP446943.RAu_Dl4EH71VLyeRZJaNtKwiQvLz8PBKd5aGEKTloYakQ130_assertion
;
np:hasProvenance
dgn-np:NP446943.RAu_Dl4EH71VLyeRZJaNtKwiQvLz8PBKd5aGEKTloYakQ130_provenance
;
np:hasPublicationInfo
dgn-np:NP446943.RAu_Dl4EH71VLyeRZJaNtKwiQvLz8PBKd5aGEKTloYakQ130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP446943.RAu_Dl4EH71VLyeRZJaNtKwiQvLz8PBKd5aGEKTloYakQ130_assertion
a
np:Assertion
.
dgn-np:NP446943.RAu_Dl4EH71VLyeRZJaNtKwiQvLz8PBKd5aGEKTloYakQ130_provenance
a
np:Provenance
.
dgn-np:NP446943.RAu_Dl4EH71VLyeRZJaNtKwiQvLz8PBKd5aGEKTloYakQ130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP446943.RAu_Dl4EH71VLyeRZJaNtKwiQvLz8PBKd5aGEKTloYakQ130_assertion
{
miriam-gene:148738
a
ncit:C16612
.
lld:C0162566
a
ncit:C7057
.
dgn-gda:DGNc124a3aa2440b5237f1d85d000298390
sio:SIO_000628
miriam-gene:148738
,
lld:C0162566
;
a
sio:SIO_001121
.
}
dgn-np:NP446943.RAu_Dl4EH71VLyeRZJaNtKwiQvLz8PBKd5aGEKTloYakQ130_provenance
{
dgn-np:NP446943.RAu_Dl4EH71VLyeRZJaNtKwiQvLz8PBKd5aGEKTloYakQ130_assertion
dcterms:description
"[To determine if mutations in or expression of these genes influenced iron overload in PCT, we compared sequences of HAMP and HJV in 96 patients with PCT and 88 HFE C282Y homozygotes with marked hepatic 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:18809758
;
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:NP446943.RAu_Dl4EH71VLyeRZJaNtKwiQvLz8PBKd5aGEKTloYakQ130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:26+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" .
}