@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP819016.RApQAnanQlIfDj5mBvx6vsqMim4wsPX63HqwPWh2KraPc
> .
@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:NP819016.RApQAnanQlIfDj5mBvx6vsqMim4wsPX63HqwPWh2KraPc130_head
{
this:
np:hasAssertion
dgn-np:NP819016.RApQAnanQlIfDj5mBvx6vsqMim4wsPX63HqwPWh2KraPc130_assertion
;
np:hasProvenance
dgn-np:NP819016.RApQAnanQlIfDj5mBvx6vsqMim4wsPX63HqwPWh2KraPc130_provenance
;
np:hasPublicationInfo
dgn-np:NP819016.RApQAnanQlIfDj5mBvx6vsqMim4wsPX63HqwPWh2KraPc130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP819016.RApQAnanQlIfDj5mBvx6vsqMim4wsPX63HqwPWh2KraPc130_assertion
a
np:Assertion
.
dgn-np:NP819016.RApQAnanQlIfDj5mBvx6vsqMim4wsPX63HqwPWh2KraPc130_provenance
a
np:Provenance
.
dgn-np:NP819016.RApQAnanQlIfDj5mBvx6vsqMim4wsPX63HqwPWh2KraPc130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP819016.RApQAnanQlIfDj5mBvx6vsqMim4wsPX63HqwPWh2KraPc130_assertion
{
miriam-gene:847
a
ncit:C16612
.
lld:C2931868
a
ncit:C7057
.
dgn-gda:DGNd190f6b46ba271cf1064d1f4c872391a
sio:SIO_000628
miriam-gene:847
,
lld:C2931868
;
a
sio:SIO_001121
.
}
dgn-np:NP819016.RApQAnanQlIfDj5mBvx6vsqMim4wsPX63HqwPWh2KraPc130_provenance
{
dgn-np:NP819016.RApQAnanQlIfDj5mBvx6vsqMim4wsPX63HqwPWh2KraPc130_assertion
dcterms:description
"[Decreases in catalase activity in patients with tumors is more likely to be due to decreased enzyme synthesis rather than to catalase mutations.Acatalasemia, the inherited deficiency of catalase has been detected in 11 countries.]. 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:15771551
;
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:NP819016.RApQAnanQlIfDj5mBvx6vsqMim4wsPX63HqwPWh2KraPc130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:21+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" .
}