@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP901885.RA0ETCx7Bjz6XtiTKyQHA7_HkGsjefeSNqxYMrBtuNOjc
> .
@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:NP901885.RA0ETCx7Bjz6XtiTKyQHA7_HkGsjefeSNqxYMrBtuNOjc130_head
{
this:
np:hasAssertion
dgn-np:NP901885.RA0ETCx7Bjz6XtiTKyQHA7_HkGsjefeSNqxYMrBtuNOjc130_assertion
;
np:hasProvenance
dgn-np:NP901885.RA0ETCx7Bjz6XtiTKyQHA7_HkGsjefeSNqxYMrBtuNOjc130_provenance
;
np:hasPublicationInfo
dgn-np:NP901885.RA0ETCx7Bjz6XtiTKyQHA7_HkGsjefeSNqxYMrBtuNOjc130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP901885.RA0ETCx7Bjz6XtiTKyQHA7_HkGsjefeSNqxYMrBtuNOjc130_assertion
a
np:Assertion
.
dgn-np:NP901885.RA0ETCx7Bjz6XtiTKyQHA7_HkGsjefeSNqxYMrBtuNOjc130_provenance
a
np:Provenance
.
dgn-np:NP901885.RA0ETCx7Bjz6XtiTKyQHA7_HkGsjefeSNqxYMrBtuNOjc130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP901885.RA0ETCx7Bjz6XtiTKyQHA7_HkGsjefeSNqxYMrBtuNOjc130_assertion
{
miriam-gene:7124
a
ncit:C16612
.
lld:C0038644
a
ncit:C7057
.
dgn-gda:DGN6ffcaef95bf3761046ad0a2ca9aeff8d
sio:SIO_000628
miriam-gene:7124
,
lld:C0038644
;
a
sio:SIO_001121
.
}
dgn-np:NP901885.RA0ETCx7Bjz6XtiTKyQHA7_HkGsjefeSNqxYMrBtuNOjc130_provenance
{
dgn-np:NP901885.RA0ETCx7Bjz6XtiTKyQHA7_HkGsjefeSNqxYMrBtuNOjc130_assertion
dcterms:description
"[Several studies indicate that interleukin gene polymorphisms are of importance to sudden infant death syndrome (SIDS), and so far it has been reported that associations between SIDS and polymorphism in the genes encoding tumor necrosis factor alpha, IL (interleukin)-6, and IL-10.]. 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:20080142
;
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:NP901885.RA0ETCx7Bjz6XtiTKyQHA7_HkGsjefeSNqxYMrBtuNOjc130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:41:14+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" .
}