@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP711724.RAqrolk42Xs5hzKWSMHawR5zMt4BXErri5HmAvv2A9WTE
> .
@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:NP711724.RAqrolk42Xs5hzKWSMHawR5zMt4BXErri5HmAvv2A9WTE130_head
{
this:
np:hasAssertion
dgn-np:NP711724.RAqrolk42Xs5hzKWSMHawR5zMt4BXErri5HmAvv2A9WTE130_assertion
;
np:hasProvenance
dgn-np:NP711724.RAqrolk42Xs5hzKWSMHawR5zMt4BXErri5HmAvv2A9WTE130_provenance
;
np:hasPublicationInfo
dgn-np:NP711724.RAqrolk42Xs5hzKWSMHawR5zMt4BXErri5HmAvv2A9WTE130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP711724.RAqrolk42Xs5hzKWSMHawR5zMt4BXErri5HmAvv2A9WTE130_assertion
a
np:Assertion
.
dgn-np:NP711724.RAqrolk42Xs5hzKWSMHawR5zMt4BXErri5HmAvv2A9WTE130_provenance
a
np:Provenance
.
dgn-np:NP711724.RAqrolk42Xs5hzKWSMHawR5zMt4BXErri5HmAvv2A9WTE130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP711724.RAqrolk42Xs5hzKWSMHawR5zMt4BXErri5HmAvv2A9WTE130_assertion
{
miriam-gene:9189
a
ncit:C16612
.
lld:C0520679
a
ncit:C7057
.
dgn-gda:DGN2d9d8203dfecaa992abd31887e02d84d
sio:SIO_000628
miriam-gene:9189
,
lld:C0520679
;
a
sio:SIO_001121
.
}
dgn-np:NP711724.RAqrolk42Xs5hzKWSMHawR5zMt4BXErri5HmAvv2A9WTE130_provenance
{
dgn-np:NP711724.RAqrolk42Xs5hzKWSMHawR5zMt4BXErri5HmAvv2A9WTE130_assertion
dcterms:description
"[We conclude that infants of families with multiple histories of SIDS, ALTE, and OSA are more likely to have OSA than infants of families with only one case of SIDS or ALTE.]. 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:10700687
;
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:NP711724.RAqrolk42Xs5hzKWSMHawR5zMt4BXErri5HmAvv2A9WTE130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:12+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" .
}