@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP60074.RATyvSvzCzskgu9816H2QynyaRfjERbMih6Z3k-NOYtv0
> .
@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:NP60074.RATyvSvzCzskgu9816H2QynyaRfjERbMih6Z3k-NOYtv0130_head
{
this:
np:hasAssertion
dgn-np:NP60074.RATyvSvzCzskgu9816H2QynyaRfjERbMih6Z3k-NOYtv0130_assertion
;
np:hasProvenance
dgn-np:NP60074.RATyvSvzCzskgu9816H2QynyaRfjERbMih6Z3k-NOYtv0130_provenance
;
np:hasPublicationInfo
dgn-np:NP60074.RATyvSvzCzskgu9816H2QynyaRfjERbMih6Z3k-NOYtv0130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP60074.RATyvSvzCzskgu9816H2QynyaRfjERbMih6Z3k-NOYtv0130_assertion
a
np:Assertion
.
dgn-np:NP60074.RATyvSvzCzskgu9816H2QynyaRfjERbMih6Z3k-NOYtv0130_provenance
a
np:Provenance
.
dgn-np:NP60074.RATyvSvzCzskgu9816H2QynyaRfjERbMih6Z3k-NOYtv0130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP60074.RATyvSvzCzskgu9816H2QynyaRfjERbMih6Z3k-NOYtv0130_assertion
{
miriam-gene:1576
a
ncit:C16612
.
lld:C0020538
a
ncit:C7057
.
dgn-gda:DGN217aac7ac69e6bc7844ec387b6121584
sio:SIO_000628
miriam-gene:1576
,
lld:C0020538
;
a
sio:SIO_001122
.
}
dgn-np:NP60074.RATyvSvzCzskgu9816H2QynyaRfjERbMih6Z3k-NOYtv0130_provenance
{
dgn-np:NP60074.RATyvSvzCzskgu9816H2QynyaRfjERbMih6Z3k-NOYtv0130_assertion
dcterms:description
"[We predict that individuals who are homozygous for defective alleles of both of these genes would metabolize CYP3A substrates poorly. The new genetic tests will be useful in future clinical studies to investigate genotype/phenotype associations.]. 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:15634941
;
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 .
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dgn-np:NP60074.RATyvSvzCzskgu9816H2QynyaRfjERbMih6Z3k-NOYtv0130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:28+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" .
}