@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP63162.RAa2J-s8eIcy6sgqihJmQNbytnaQudhde5aVeyMUcSi5s
> .
@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:NP63162.RAa2J-s8eIcy6sgqihJmQNbytnaQudhde5aVeyMUcSi5s130_head
{
this:
np:hasAssertion
dgn-np:NP63162.RAa2J-s8eIcy6sgqihJmQNbytnaQudhde5aVeyMUcSi5s130_assertion
;
np:hasProvenance
dgn-np:NP63162.RAa2J-s8eIcy6sgqihJmQNbytnaQudhde5aVeyMUcSi5s130_provenance
;
np:hasPublicationInfo
dgn-np:NP63162.RAa2J-s8eIcy6sgqihJmQNbytnaQudhde5aVeyMUcSi5s130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP63162.RAa2J-s8eIcy6sgqihJmQNbytnaQudhde5aVeyMUcSi5s130_assertion
a
np:Assertion
.
dgn-np:NP63162.RAa2J-s8eIcy6sgqihJmQNbytnaQudhde5aVeyMUcSi5s130_provenance
a
np:Provenance
.
dgn-np:NP63162.RAa2J-s8eIcy6sgqihJmQNbytnaQudhde5aVeyMUcSi5s130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP63162.RAa2J-s8eIcy6sgqihJmQNbytnaQudhde5aVeyMUcSi5s130_assertion
{
miriam-gene:1586
a
ncit:C16612
.
lld:C0023895
a
ncit:C7057
.
dgn-gda:DGNab190a5fdd4b2f78cfa199ab6c81cf23
sio:SIO_000628
miriam-gene:1586
,
lld:C0023895
;
a
sio:SIO_001122
.
}
dgn-np:NP63162.RAa2J-s8eIcy6sgqihJmQNbytnaQudhde5aVeyMUcSi5s130_provenance
{
dgn-np:NP63162.RAa2J-s8eIcy6sgqihJmQNbytnaQudhde5aVeyMUcSi5s130_assertion
dcterms:description
"[Our study provides the first evidence that CYP17 polymorphism participates in the development of THS, and sheds light on the genetic causes of this side effect and genetic differences between tamoxifen-treated individuals.]. 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:15706422
;
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:NP63162.RAa2J-s8eIcy6sgqihJmQNbytnaQudhde5aVeyMUcSi5s130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:30+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" .
}