@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP431900.RAV6IuRw-IC1MX0SASsnxhU_r0flZEk2P23hwuZ_kE7co
> .
@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:NP431900.RAV6IuRw-IC1MX0SASsnxhU_r0flZEk2P23hwuZ_kE7co130_head
{
this:
np:hasAssertion
dgn-np:NP431900.RAV6IuRw-IC1MX0SASsnxhU_r0flZEk2P23hwuZ_kE7co130_assertion
;
np:hasProvenance
dgn-np:NP431900.RAV6IuRw-IC1MX0SASsnxhU_r0flZEk2P23hwuZ_kE7co130_provenance
;
np:hasPublicationInfo
dgn-np:NP431900.RAV6IuRw-IC1MX0SASsnxhU_r0flZEk2P23hwuZ_kE7co130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP431900.RAV6IuRw-IC1MX0SASsnxhU_r0flZEk2P23hwuZ_kE7co130_assertion
a
np:Assertion
.
dgn-np:NP431900.RAV6IuRw-IC1MX0SASsnxhU_r0flZEk2P23hwuZ_kE7co130_provenance
a
np:Provenance
.
dgn-np:NP431900.RAV6IuRw-IC1MX0SASsnxhU_r0flZEk2P23hwuZ_kE7co130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP431900.RAV6IuRw-IC1MX0SASsnxhU_r0flZEk2P23hwuZ_kE7co130_assertion
{
miriam-gene:3077
a
ncit:C16612
.
lld:C0019202
a
ncit:C7057
.
dgn-gda:DGN7faa2f7f9040f8264b02027c20f7dc1c
sio:SIO_000628
miriam-gene:3077
,
lld:C0019202
;
a
sio:SIO_001121
.
}
dgn-np:NP431900.RAV6IuRw-IC1MX0SASsnxhU_r0flZEk2P23hwuZ_kE7co130_provenance
{
dgn-np:NP431900.RAV6IuRw-IC1MX0SASsnxhU_r0flZEk2P23hwuZ_kE7co130_assertion
dcterms:description
"[This review of the copper-iron interaction in Wilson's disease was mainly based on ten patients (three females and seven males) studied in our institutes because the genetic tests of ATP7B for Wilson's disease of primary copper toxicosis and HFE for hemochromatosis, the biochemical parameters of copper and iron, and morphological studies on biopsied liver specimens were complete.]. 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:16998622
;
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:NP431900.RAV6IuRw-IC1MX0SASsnxhU_r0flZEk2P23hwuZ_kE7co130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:16+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" .
}