@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP361496.RARCyAFnQBQ64jE-BxNQ_yjNH8kNB6SqL1AW0qT2A3Ims
> .
@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:NP361496.RARCyAFnQBQ64jE-BxNQ_yjNH8kNB6SqL1AW0qT2A3Ims130_head
{
this:
np:hasAssertion
dgn-np:NP361496.RARCyAFnQBQ64jE-BxNQ_yjNH8kNB6SqL1AW0qT2A3Ims130_assertion
;
np:hasProvenance
dgn-np:NP361496.RARCyAFnQBQ64jE-BxNQ_yjNH8kNB6SqL1AW0qT2A3Ims130_provenance
;
np:hasPublicationInfo
dgn-np:NP361496.RARCyAFnQBQ64jE-BxNQ_yjNH8kNB6SqL1AW0qT2A3Ims130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP361496.RARCyAFnQBQ64jE-BxNQ_yjNH8kNB6SqL1AW0qT2A3Ims130_assertion
a
np:Assertion
.
dgn-np:NP361496.RARCyAFnQBQ64jE-BxNQ_yjNH8kNB6SqL1AW0qT2A3Ims130_provenance
a
np:Provenance
.
dgn-np:NP361496.RARCyAFnQBQ64jE-BxNQ_yjNH8kNB6SqL1AW0qT2A3Ims130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP361496.RARCyAFnQBQ64jE-BxNQ_yjNH8kNB6SqL1AW0qT2A3Ims130_assertion
{
miriam-gene:2950
a
ncit:C16612
.
lld:C0014850
a
ncit:C7057
.
dgn-gda:DGN94915e881219b9ddffc578aa2966563f
sio:SIO_000628
miriam-gene:2950
,
lld:C0014850
;
a
sio:SIO_001121
.
}
dgn-np:NP361496.RARCyAFnQBQ64jE-BxNQ_yjNH8kNB6SqL1AW0qT2A3Ims130_provenance
{
dgn-np:NP361496.RARCyAFnQBQ64jE-BxNQ_yjNH8kNB6SqL1AW0qT2A3Ims130_assertion
dcterms:description
"[We hypothesize that the deletion of one GSTP1 allele (an isoform highly expressed in embryonic tissues), associated with specific environmental factors, such as tobacco and alcohol, could cause the esophageal atresia observed in our patient.]. 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:23828841
;
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:NP361496.RARCyAFnQBQ64jE-BxNQ_yjNH8kNB6SqL1AW0qT2A3Ims130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:32+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" .
}