@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP742878.RAxucobnfUBue-2SXH9YUJ7cy2zVV7Ny9gAwIlyojT5l4
> .
@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:NP742878.RAxucobnfUBue-2SXH9YUJ7cy2zVV7Ny9gAwIlyojT5l4130_head
{
this:
np:hasAssertion
dgn-np:NP742878.RAxucobnfUBue-2SXH9YUJ7cy2zVV7Ny9gAwIlyojT5l4130_assertion
;
np:hasProvenance
dgn-np:NP742878.RAxucobnfUBue-2SXH9YUJ7cy2zVV7Ny9gAwIlyojT5l4130_provenance
;
np:hasPublicationInfo
dgn-np:NP742878.RAxucobnfUBue-2SXH9YUJ7cy2zVV7Ny9gAwIlyojT5l4130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP742878.RAxucobnfUBue-2SXH9YUJ7cy2zVV7Ny9gAwIlyojT5l4130_assertion
a
np:Assertion
.
dgn-np:NP742878.RAxucobnfUBue-2SXH9YUJ7cy2zVV7Ny9gAwIlyojT5l4130_provenance
a
np:Provenance
.
dgn-np:NP742878.RAxucobnfUBue-2SXH9YUJ7cy2zVV7Ny9gAwIlyojT5l4130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP742878.RAxucobnfUBue-2SXH9YUJ7cy2zVV7Ny9gAwIlyojT5l4130_assertion
{
miriam-gene:6648
a
ncit:C16612
.
lld:C0007222
a
ncit:C7057
.
dgn-gda:DGNc7e3742dc169fac8fc5802764aeb4be5
sio:SIO_000628
miriam-gene:6648
,
lld:C0007222
;
a
sio:SIO_001121
.
}
dgn-np:NP742878.RAxucobnfUBue-2SXH9YUJ7cy2zVV7Ny9gAwIlyojT5l4130_provenance
{
dgn-np:NP742878.RAxucobnfUBue-2SXH9YUJ7cy2zVV7Ny9gAwIlyojT5l4130_assertion
dcterms:description
"[Although the majority of evidence supports associations between the SOD2 Ala16Val SNP and diseases such as breast, prostate and lung cancers, diabetes and cardiovascular disease, the presence of the SOD2 Ala16Val SNP confers only a small, clinically insignificant reduction (if any) in the risk of these diseases.]. 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:22525041
;
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:NP742878.RAxucobnfUBue-2SXH9YUJ7cy2zVV7Ny9gAwIlyojT5l4130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:30+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" .
}