@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP607776.RAnflxdun_MC4F5YePNGu13fU7Zde2YYg2fjsO3-kL7No
> .
@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:NP607776.RAnflxdun_MC4F5YePNGu13fU7Zde2YYg2fjsO3-kL7No130_head
{
this:
np:hasAssertion
dgn-np:NP607776.RAnflxdun_MC4F5YePNGu13fU7Zde2YYg2fjsO3-kL7No130_assertion
;
np:hasProvenance
dgn-np:NP607776.RAnflxdun_MC4F5YePNGu13fU7Zde2YYg2fjsO3-kL7No130_provenance
;
np:hasPublicationInfo
dgn-np:NP607776.RAnflxdun_MC4F5YePNGu13fU7Zde2YYg2fjsO3-kL7No130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP607776.RAnflxdun_MC4F5YePNGu13fU7Zde2YYg2fjsO3-kL7No130_assertion
a
np:Assertion
.
dgn-np:NP607776.RAnflxdun_MC4F5YePNGu13fU7Zde2YYg2fjsO3-kL7No130_provenance
a
np:Provenance
.
dgn-np:NP607776.RAnflxdun_MC4F5YePNGu13fU7Zde2YYg2fjsO3-kL7No130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP607776.RAnflxdun_MC4F5YePNGu13fU7Zde2YYg2fjsO3-kL7No130_assertion
{
miriam-gene:6647
a
ncit:C16612
.
lld:C0004096
a
ncit:C7057
.
dgn-gda:DGN875d305036f4357b0b5358a52b09e662
sio:SIO_000628
miriam-gene:6647
,
lld:C0004096
;
a
sio:SIO_001121
.
}
dgn-np:NP607776.RAnflxdun_MC4F5YePNGu13fU7Zde2YYg2fjsO3-kL7No130_provenance
{
dgn-np:NP607776.RAnflxdun_MC4F5YePNGu13fU7Zde2YYg2fjsO3-kL7No130_assertion
dcterms:description
"[The allele frequencies of two missense polymorphisms of SOD genes (Ala16Val in MnSOD (SOD2) and Arg213Gly in ECSOD (SOD3)) were investigated in Finnish patients with asthma and compared with family based controls.]. 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:14760150
;
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:NP607776.RAnflxdun_MC4F5YePNGu13fU7Zde2YYg2fjsO3-kL7No130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:05+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" .
}