@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP444804.RAGl3HDRY5GP0n1kDTMEbj_OJmB7_KB6i7Iz5YURZMd2E
> .
@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:NP444804.RAGl3HDRY5GP0n1kDTMEbj_OJmB7_KB6i7Iz5YURZMd2E130_head
{
this:
np:hasAssertion
dgn-np:NP444804.RAGl3HDRY5GP0n1kDTMEbj_OJmB7_KB6i7Iz5YURZMd2E130_assertion
;
np:hasProvenance
dgn-np:NP444804.RAGl3HDRY5GP0n1kDTMEbj_OJmB7_KB6i7Iz5YURZMd2E130_provenance
;
np:hasPublicationInfo
dgn-np:NP444804.RAGl3HDRY5GP0n1kDTMEbj_OJmB7_KB6i7Iz5YURZMd2E130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP444804.RAGl3HDRY5GP0n1kDTMEbj_OJmB7_KB6i7Iz5YURZMd2E130_assertion
a
np:Assertion
.
dgn-np:NP444804.RAGl3HDRY5GP0n1kDTMEbj_OJmB7_KB6i7Iz5YURZMd2E130_provenance
a
np:Provenance
.
dgn-np:NP444804.RAGl3HDRY5GP0n1kDTMEbj_OJmB7_KB6i7Iz5YURZMd2E130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP444804.RAGl3HDRY5GP0n1kDTMEbj_OJmB7_KB6i7Iz5YURZMd2E130_assertion
{
miriam-gene:1728
a
ncit:C16612
.
lld:C0004096
a
ncit:C7057
.
dgn-gda:DGN8df3669a0ffc6fbbb18cf0dd3203499c
sio:SIO_000628
miriam-gene:1728
,
lld:C0004096
;
a
sio:SIO_001121
.
}
dgn-np:NP444804.RAGl3HDRY5GP0n1kDTMEbj_OJmB7_KB6i7Iz5YURZMd2E130_provenance
{
dgn-np:NP444804.RAGl3HDRY5GP0n1kDTMEbj_OJmB7_KB6i7Iz5YURZMd2E130_assertion
dcterms:description
"[Our study supports the role of NQO1 polymorphism as an important factor determining the intensity of medical therapy in asthmatic children after adjusting for significance relating to parental income and education level, age, and restricted physical activity.]. 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:19027876
;
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:NP444804.RAGl3HDRY5GP0n1kDTMEbj_OJmB7_KB6i7Iz5YURZMd2E130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:25+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" .
}