@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP342097.RAAlMbxiOqexPIgZNCmCu0Gdg0Ci0BEeFL1Ptx8TwzjSs
> .
@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:NP342097.RAAlMbxiOqexPIgZNCmCu0Gdg0Ci0BEeFL1Ptx8TwzjSs130_head
{
this:
np:hasAssertion
dgn-np:NP342097.RAAlMbxiOqexPIgZNCmCu0Gdg0Ci0BEeFL1Ptx8TwzjSs130_assertion
;
np:hasProvenance
dgn-np:NP342097.RAAlMbxiOqexPIgZNCmCu0Gdg0Ci0BEeFL1Ptx8TwzjSs130_provenance
;
np:hasPublicationInfo
dgn-np:NP342097.RAAlMbxiOqexPIgZNCmCu0Gdg0Ci0BEeFL1Ptx8TwzjSs130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP342097.RAAlMbxiOqexPIgZNCmCu0Gdg0Ci0BEeFL1Ptx8TwzjSs130_assertion
a
np:Assertion
.
dgn-np:NP342097.RAAlMbxiOqexPIgZNCmCu0Gdg0Ci0BEeFL1Ptx8TwzjSs130_provenance
a
np:Provenance
.
dgn-np:NP342097.RAAlMbxiOqexPIgZNCmCu0Gdg0Ci0BEeFL1Ptx8TwzjSs130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP342097.RAAlMbxiOqexPIgZNCmCu0Gdg0Ci0BEeFL1Ptx8TwzjSs130_assertion
{
miriam-gene:5530
a
ncit:C16612
.
lld:C0006142
a
ncit:C7057
.
dgn-gda:DGNbbbdc80288c484e186403df68f69712d
sio:SIO_000628
miriam-gene:5530
,
lld:C0006142
;
a
sio:SIO_001121
.
}
dgn-np:NP342097.RAAlMbxiOqexPIgZNCmCu0Gdg0Ci0BEeFL1Ptx8TwzjSs130_provenance
{
dgn-np:NP342097.RAAlMbxiOqexPIgZNCmCu0Gdg0Ci0BEeFL1Ptx8TwzjSs130_assertion
dcterms:description
"[This study aimed to validate matrix-assisted laser desorption/ionization-time-of-flight mass spectrometry (MALDI-TOF MS)/Taqman copy number assay (CNA) CYP2D6 genotyping by AmpliChip CYP450 Test for the prediction of tamoxifen metabolizer phenotypes in breast cancer, and to investigate the influence of CYP2D6 variant coverage on genotype-phenotype relationships and tamoxifen outcome.]. 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:20515869
;
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:NP342097.RAAlMbxiOqexPIgZNCmCu0Gdg0Ci0BEeFL1Ptx8TwzjSs130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:21+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" .
}