@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP345840.RA1i7LadtPf9l3XEQz1-umDFPdlGK1HjlrehJj2J4GROA
> .
@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:NP345840.RA1i7LadtPf9l3XEQz1-umDFPdlGK1HjlrehJj2J4GROA130_head
{
this:
np:hasAssertion
dgn-np:NP345840.RA1i7LadtPf9l3XEQz1-umDFPdlGK1HjlrehJj2J4GROA130_assertion
;
np:hasProvenance
dgn-np:NP345840.RA1i7LadtPf9l3XEQz1-umDFPdlGK1HjlrehJj2J4GROA130_provenance
;
np:hasPublicationInfo
dgn-np:NP345840.RA1i7LadtPf9l3XEQz1-umDFPdlGK1HjlrehJj2J4GROA130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP345840.RA1i7LadtPf9l3XEQz1-umDFPdlGK1HjlrehJj2J4GROA130_assertion
a
np:Assertion
.
dgn-np:NP345840.RA1i7LadtPf9l3XEQz1-umDFPdlGK1HjlrehJj2J4GROA130_provenance
a
np:Provenance
.
dgn-np:NP345840.RA1i7LadtPf9l3XEQz1-umDFPdlGK1HjlrehJj2J4GROA130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP345840.RA1i7LadtPf9l3XEQz1-umDFPdlGK1HjlrehJj2J4GROA130_assertion
{
miriam-gene:7037
a
ncit:C16612
.
lld:C0019693
a
ncit:C7057
.
dgn-gda:DGN4dd3ca70999cccb98fb0aea7903c6096
sio:SIO_000628
miriam-gene:7037
,
lld:C0019693
;
a
sio:SIO_001121
.
}
dgn-np:NP345840.RA1i7LadtPf9l3XEQz1-umDFPdlGK1HjlrehJj2J4GROA130_provenance
{
dgn-np:NP345840.RA1i7LadtPf9l3XEQz1-umDFPdlGK1HjlrehJj2J4GROA130_assertion
dcterms:description
"[To evaluate the incidence and spectrum of HFE mutations and the relative frequency of the two main alleles of transferrin receptor in patients with PCT originating from southern France, and to evaluate the relationship of these genetic data with iron status, and with hepatitis B and C and human immunodeficiency virus (HIV) infections.]. 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:11260010
;
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:NP345840.RA1i7LadtPf9l3XEQz1-umDFPdlGK1HjlrehJj2J4GROA130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:23+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" .
}