@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP688073.RAlDYp5wUpSAqA1Sfw8qLKXxPGmpD5ORAYDNTkBQUGaRU
> .
@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:NP688073.RAlDYp5wUpSAqA1Sfw8qLKXxPGmpD5ORAYDNTkBQUGaRU130_head
{
this:
np:hasAssertion
dgn-np:NP688073.RAlDYp5wUpSAqA1Sfw8qLKXxPGmpD5ORAYDNTkBQUGaRU130_assertion
;
np:hasProvenance
dgn-np:NP688073.RAlDYp5wUpSAqA1Sfw8qLKXxPGmpD5ORAYDNTkBQUGaRU130_provenance
;
np:hasPublicationInfo
dgn-np:NP688073.RAlDYp5wUpSAqA1Sfw8qLKXxPGmpD5ORAYDNTkBQUGaRU130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP688073.RAlDYp5wUpSAqA1Sfw8qLKXxPGmpD5ORAYDNTkBQUGaRU130_assertion
a
np:Assertion
.
dgn-np:NP688073.RAlDYp5wUpSAqA1Sfw8qLKXxPGmpD5ORAYDNTkBQUGaRU130_provenance
a
np:Provenance
.
dgn-np:NP688073.RAlDYp5wUpSAqA1Sfw8qLKXxPGmpD5ORAYDNTkBQUGaRU130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP688073.RAlDYp5wUpSAqA1Sfw8qLKXxPGmpD5ORAYDNTkBQUGaRU130_assertion
{
miriam-gene:3077
a
ncit:C16612
.
lld:C0524620
a
ncit:C7057
.
dgn-gda:DGNa3ff7237ddda135019c0b1a0f31e1b74
sio:SIO_000628
miriam-gene:3077
,
lld:C0524620
;
a
sio:SIO_001121
.
}
dgn-np:NP688073.RAlDYp5wUpSAqA1Sfw8qLKXxPGmpD5ORAYDNTkBQUGaRU130_provenance
{
dgn-np:NP688073.RAlDYp5wUpSAqA1Sfw8qLKXxPGmpD5ORAYDNTkBQUGaRU130_assertion
dcterms:description
"[For clinicians, the challenge is now to diagnose HH before irreversible damage develops and, at the same time, to distinguish progressive iron overload from increasingly common diseases with only moderately increased body iron stores, such as the metabolic syndrome.]. 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:16627556
;
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:NP688073.RAlDYp5wUpSAqA1Sfw8qLKXxPGmpD5ORAYDNTkBQUGaRU130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:58+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" .
}