@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP364319.RApzaQpg0YZ36crUcjoUWOxnYq9zTGtNrifFSeEY0ELms
> .
@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:NP364319.RApzaQpg0YZ36crUcjoUWOxnYq9zTGtNrifFSeEY0ELms130_head
{
this:
np:hasAssertion
dgn-np:NP364319.RApzaQpg0YZ36crUcjoUWOxnYq9zTGtNrifFSeEY0ELms130_assertion
;
np:hasProvenance
dgn-np:NP364319.RApzaQpg0YZ36crUcjoUWOxnYq9zTGtNrifFSeEY0ELms130_provenance
;
np:hasPublicationInfo
dgn-np:NP364319.RApzaQpg0YZ36crUcjoUWOxnYq9zTGtNrifFSeEY0ELms130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP364319.RApzaQpg0YZ36crUcjoUWOxnYq9zTGtNrifFSeEY0ELms130_assertion
a
np:Assertion
.
dgn-np:NP364319.RApzaQpg0YZ36crUcjoUWOxnYq9zTGtNrifFSeEY0ELms130_provenance
a
np:Provenance
.
dgn-np:NP364319.RApzaQpg0YZ36crUcjoUWOxnYq9zTGtNrifFSeEY0ELms130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP364319.RApzaQpg0YZ36crUcjoUWOxnYq9zTGtNrifFSeEY0ELms130_assertion
{
miriam-gene:4128
a
ncit:C16612
.
lld:C0027497
a
ncit:C7057
.
dgn-gda:DGNa1e40c1dc2c41a4262c95d55ee52d007
sio:SIO_000628
miriam-gene:4128
,
lld:C0027497
;
a
sio:SIO_001121
.
}
dgn-np:NP364319.RApzaQpg0YZ36crUcjoUWOxnYq9zTGtNrifFSeEY0ELms130_provenance
{
dgn-np:NP364319.RApzaQpg0YZ36crUcjoUWOxnYq9zTGtNrifFSeEY0ELms130_assertion
dcterms:description
"[The frequency of MAOA-VNTR allele 1 was significantly higher in the patients without nausea than in ones with nausea in the statistical analysis including the patients whose plasma levels were below the average and who were considered to be pharmacodynamically more sensitive to nausea.]. 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:12886034
;
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:NP364319.RApzaQpg0YZ36crUcjoUWOxnYq9zTGtNrifFSeEY0ELms130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:33+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" .
}