@prefix dct: <
http://purl.org/dc/terms/
> .
@prefix orcid: <
http://orcid.org/
> .
@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP43935.RAq8C2UCo1wOe-Ko7dhGi7yGf9y43Lesr5qWRAUqXcOl8
> .
@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 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:NP43935.RAq8C2UCo1wOe-Ko7dhGi7yGf9y43Lesr5qWRAUqXcOl8130_head
{
this:
np:hasAssertion
dgn-np:NP43935.RAq8C2UCo1wOe-Ko7dhGi7yGf9y43Lesr5qWRAUqXcOl8130_assertion
;
np:hasProvenance
dgn-np:NP43935.RAq8C2UCo1wOe-Ko7dhGi7yGf9y43Lesr5qWRAUqXcOl8130_provenance
;
np:hasPublicationInfo
dgn-np:NP43935.RAq8C2UCo1wOe-Ko7dhGi7yGf9y43Lesr5qWRAUqXcOl8130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP43935.RAq8C2UCo1wOe-Ko7dhGi7yGf9y43Lesr5qWRAUqXcOl8130_assertion
a
np:Assertion
.
dgn-np:NP43935.RAq8C2UCo1wOe-Ko7dhGi7yGf9y43Lesr5qWRAUqXcOl8130_provenance
a
np:Provenance
.
dgn-np:NP43935.RAq8C2UCo1wOe-Ko7dhGi7yGf9y43Lesr5qWRAUqXcOl8130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP43935.RAq8C2UCo1wOe-Ko7dhGi7yGf9y43Lesr5qWRAUqXcOl8130_assertion
{
miriam-gene:2328
a
ncit:C16612
.
lld:C0020538
a
ncit:C7057
.
dgn-gda:DGN685ce21ae2b45696e8dab1ec63c939be
sio:SIO_000628
miriam-gene:2328
,
lld:C0020538
;
a
sio:SIO_001122
.
}
dgn-np:NP43935.RAq8C2UCo1wOe-Ko7dhGi7yGf9y43Lesr5qWRAUqXcOl8130_provenance
{
dgn-np:NP43935.RAq8C2UCo1wOe-Ko7dhGi7yGf9y43Lesr5qWRAUqXcOl8130_assertion
dct:description
"[tatistically significant heterogeneity in the relative frequencies of single and multiple site alleles, haplotypes, and genotypes of the human FMO3 among ethnic subdivisions suggests that population differences in the susceptibility of humans to abnormal metabolism or adverse drug reactions for chemicals metabolized by human FMO3 could exist.]. 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:11717182
;
prov:wasDerivedFrom
dgn-void:gad-20130706
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:gad-20130706
pav:importedOn
"2013-07-06"^^
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:NP43935.RAq8C2UCo1wOe-Ko7dhGi7yGf9y43Lesr5qWRAUqXcOl8130_publicationInfo
{
this:
dct:created
"2014-10-02T12:32:20+02:00"^^
xsd:dateTime
;
dct:rights
<
http://opendatacommons.org/licenses/odbl/1.0/
> ;
dct:rightsHolder
dgn-void:IBIGroup
;
dct:subject
sio:SIO_000983
;
prv:usedData
dgn-void:disgenetrdf
;
pav:authoredBy
orcid:0000-0001-5999-6269
,
orcid:0000-0002-7534-7661
,
orcid:0000-0002-9383-528X
,
orcid:0000-0003-0169-8159
,
orcid:0000-0003-1244-7654
;
pav:createdBy
orcid:0000-0003-0169-8159
;
pav:version
"v2.1.0.0" .
dgn-void:disgenetrdf
pav:version
"v2.1.0" .
}