@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP761821.RA2qGn2VtYahfc4ashnfiOwWq0JMW4VV0IN_7nNrG5vr8
> .
@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:NP761821.RA2qGn2VtYahfc4ashnfiOwWq0JMW4VV0IN_7nNrG5vr8130_head
{
this:
np:hasAssertion
dgn-np:NP761821.RA2qGn2VtYahfc4ashnfiOwWq0JMW4VV0IN_7nNrG5vr8130_assertion
;
np:hasProvenance
dgn-np:NP761821.RA2qGn2VtYahfc4ashnfiOwWq0JMW4VV0IN_7nNrG5vr8130_provenance
;
np:hasPublicationInfo
dgn-np:NP761821.RA2qGn2VtYahfc4ashnfiOwWq0JMW4VV0IN_7nNrG5vr8130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP761821.RA2qGn2VtYahfc4ashnfiOwWq0JMW4VV0IN_7nNrG5vr8130_assertion
a
np:Assertion
.
dgn-np:NP761821.RA2qGn2VtYahfc4ashnfiOwWq0JMW4VV0IN_7nNrG5vr8130_provenance
a
np:Provenance
.
dgn-np:NP761821.RA2qGn2VtYahfc4ashnfiOwWq0JMW4VV0IN_7nNrG5vr8130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP761821.RA2qGn2VtYahfc4ashnfiOwWq0JMW4VV0IN_7nNrG5vr8130_assertion
{
miriam-gene:1356
a
ncit:C16612
.
lld:C0282193
a
ncit:C7057
.
dgn-gda:DGN1ae7a0424d0a773e343aec03277ca621
sio:SIO_000628
miriam-gene:1356
,
lld:C0282193
;
a
sio:SIO_001121
.
}
dgn-np:NP761821.RA2qGn2VtYahfc4ashnfiOwWq0JMW4VV0IN_7nNrG5vr8130_provenance
{
dgn-np:NP761821.RA2qGn2VtYahfc4ashnfiOwWq0JMW4VV0IN_7nNrG5vr8130_assertion
dcterms:description
"[As ceruloplasmin (Cp) seems to be involved in iron mobilization, serum Cp levels were measured in 35 patients with hereditary haemochromatosis (HH), 12 with acquired iron overload (AIO) and 36 healthy subjects.]. 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:11472372
;
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:NP761821.RA2qGn2VtYahfc4ashnfiOwWq0JMW4VV0IN_7nNrG5vr8130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:41+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" .
}