@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP468026.RA93ByTsNxQKKLJWHD717HWkIa3WzpSS9zNtwFFC1c19E
> .
@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:NP468026.RA93ByTsNxQKKLJWHD717HWkIa3WzpSS9zNtwFFC1c19E130_head
{
this:
np:hasAssertion
dgn-np:NP468026.RA93ByTsNxQKKLJWHD717HWkIa3WzpSS9zNtwFFC1c19E130_assertion
;
np:hasProvenance
dgn-np:NP468026.RA93ByTsNxQKKLJWHD717HWkIa3WzpSS9zNtwFFC1c19E130_provenance
;
np:hasPublicationInfo
dgn-np:NP468026.RA93ByTsNxQKKLJWHD717HWkIa3WzpSS9zNtwFFC1c19E130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP468026.RA93ByTsNxQKKLJWHD717HWkIa3WzpSS9zNtwFFC1c19E130_assertion
a
np:Assertion
.
dgn-np:NP468026.RA93ByTsNxQKKLJWHD717HWkIa3WzpSS9zNtwFFC1c19E130_provenance
a
np:Provenance
.
dgn-np:NP468026.RA93ByTsNxQKKLJWHD717HWkIa3WzpSS9zNtwFFC1c19E130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP468026.RA93ByTsNxQKKLJWHD717HWkIa3WzpSS9zNtwFFC1c19E130_assertion
{
miriam-gene:7982
a
ncit:C16612
.
lld:C0004096
a
ncit:C7057
.
dgn-gda:DGN99805c07473e0e6488cd549996714726
sio:SIO_000628
miriam-gene:7982
,
lld:C0004096
;
a
sio:SIO_001121
.
}
dgn-np:NP468026.RA93ByTsNxQKKLJWHD717HWkIa3WzpSS9zNtwFFC1c19E130_provenance
{
dgn-np:NP468026.RA93ByTsNxQKKLJWHD717HWkIa3WzpSS9zNtwFFC1c19E130_assertion
dcterms:description
"[Preventive treatment based on an early genetic screening of those children who present wheezing episodes during the first year of life, with treatment applied to those who test positive for the asthma-associated genetic marker ADAM33 ST+7, is theoretically cost effective.]. 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:17963419
;
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:NP468026.RA93ByTsNxQKKLJWHD717HWkIa3WzpSS9zNtwFFC1c19E130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:40+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" .
}