@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP768369.RAsw0GC-EF58C94ZdWuD-OMYRVwz-ee4DAX5_t1Gc2cWk
> .
@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:NP768369.RAsw0GC-EF58C94ZdWuD-OMYRVwz-ee4DAX5_t1Gc2cWk130_head
{
this:
np:hasAssertion
dgn-np:NP768369.RAsw0GC-EF58C94ZdWuD-OMYRVwz-ee4DAX5_t1Gc2cWk130_assertion
;
np:hasProvenance
dgn-np:NP768369.RAsw0GC-EF58C94ZdWuD-OMYRVwz-ee4DAX5_t1Gc2cWk130_provenance
;
np:hasPublicationInfo
dgn-np:NP768369.RAsw0GC-EF58C94ZdWuD-OMYRVwz-ee4DAX5_t1Gc2cWk130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP768369.RAsw0GC-EF58C94ZdWuD-OMYRVwz-ee4DAX5_t1Gc2cWk130_assertion
a
np:Assertion
.
dgn-np:NP768369.RAsw0GC-EF58C94ZdWuD-OMYRVwz-ee4DAX5_t1Gc2cWk130_provenance
a
np:Provenance
.
dgn-np:NP768369.RAsw0GC-EF58C94ZdWuD-OMYRVwz-ee4DAX5_t1Gc2cWk130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP768369.RAsw0GC-EF58C94ZdWuD-OMYRVwz-ee4DAX5_t1Gc2cWk130_assertion
{
miriam-gene:2952
a
ncit:C16612
.
lld:C0043144
a
ncit:C7057
.
dgn-gda:DGN20f623c21274093aa0ca4873af814ebc
sio:SIO_000628
miriam-gene:2952
,
lld:C0043144
;
a
sio:SIO_001121
.
}
dgn-np:NP768369.RAsw0GC-EF58C94ZdWuD-OMYRVwz-ee4DAX5_t1Gc2cWk130_provenance
{
dgn-np:NP768369.RAsw0GC-EF58C94ZdWuD-OMYRVwz-ee4DAX5_t1Gc2cWk130_assertion
dcterms:description
"[Risk of asthma associated with late gestation exposure was higher when maternal GSTT1 genotype was present rather than absent (P interaction, .006), and risk of wheezing was increased when maternal GSTM1 was present (P interaction, .04).]. 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:21051083
;
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:NP768369.RAsw0GC-EF58C94ZdWuD-OMYRVwz-ee4DAX5_t1Gc2cWk130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:45+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" .
}