@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP321600.RAVSCk4eMLRtjFOAjDPrPPPDFtxqMVof7MIRBMm2eUPpo
> .
@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/v4.0.0/void/
> .
dgn-np:NP321600.RAVSCk4eMLRtjFOAjDPrPPPDFtxqMVof7MIRBMm2eUPpo130_head
{
this:
np:hasAssertion
dgn-np:NP321600.RAVSCk4eMLRtjFOAjDPrPPPDFtxqMVof7MIRBMm2eUPpo130_assertion
;
np:hasProvenance
dgn-np:NP321600.RAVSCk4eMLRtjFOAjDPrPPPDFtxqMVof7MIRBMm2eUPpo130_provenance
;
np:hasPublicationInfo
dgn-np:NP321600.RAVSCk4eMLRtjFOAjDPrPPPDFtxqMVof7MIRBMm2eUPpo130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP321600.RAVSCk4eMLRtjFOAjDPrPPPDFtxqMVof7MIRBMm2eUPpo130_assertion
a
np:Assertion
.
dgn-np:NP321600.RAVSCk4eMLRtjFOAjDPrPPPDFtxqMVof7MIRBMm2eUPpo130_provenance
a
np:Provenance
.
dgn-np:NP321600.RAVSCk4eMLRtjFOAjDPrPPPDFtxqMVof7MIRBMm2eUPpo130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP321600.RAVSCk4eMLRtjFOAjDPrPPPDFtxqMVof7MIRBMm2eUPpo130_assertion
{
miriam-gene:2395
a
ncit:C16612
.
lld:C0282193
a
ncit:C7057
.
dgn-gda:DGN4d7eee4858d6b7007eb641d00c29099a
sio:SIO_000628
miriam-gene:2395
,
lld:C0282193
;
a
sio:SIO_001121
.
}
dgn-np:NP321600.RAVSCk4eMLRtjFOAjDPrPPPDFtxqMVof7MIRBMm2eUPpo130_provenance
{
dgn-np:NP321600.RAVSCk4eMLRtjFOAjDPrPPPDFtxqMVof7MIRBMm2eUPpo130_assertion
dcterms:description
"[Many of these disorders are characterized by iron overload and include relatively common diseases such as hereditary hemochromatosis, rare abnormalities of plasma protein synthesis (atransferrinemia and aceruloplasminemia), and the neuromuscular disease Friedreich ataxia.]. 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:11419690
;
prov:wasDerivedFrom
dgn-void:befree-2016
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-2016
pav:importedOn
"2016-02-19"^^
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:NP321600.RAVSCk4eMLRtjFOAjDPrPPPDFtxqMVof7MIRBMm2eUPpo130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:44:11+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
"v4.0.0.0" .
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pav:version
"v4.0.0" .
}