@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP847109.RAAdivqJVKhDWAqaFF1b2bk3e9A8pkCWJDfmPPFcm1hFM
> .
@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:NP847109.RAAdivqJVKhDWAqaFF1b2bk3e9A8pkCWJDfmPPFcm1hFM130_head
{
this:
np:hasAssertion
dgn-np:NP847109.RAAdivqJVKhDWAqaFF1b2bk3e9A8pkCWJDfmPPFcm1hFM130_assertion
;
np:hasProvenance
dgn-np:NP847109.RAAdivqJVKhDWAqaFF1b2bk3e9A8pkCWJDfmPPFcm1hFM130_provenance
;
np:hasPublicationInfo
dgn-np:NP847109.RAAdivqJVKhDWAqaFF1b2bk3e9A8pkCWJDfmPPFcm1hFM130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP847109.RAAdivqJVKhDWAqaFF1b2bk3e9A8pkCWJDfmPPFcm1hFM130_assertion
a
np:Assertion
.
dgn-np:NP847109.RAAdivqJVKhDWAqaFF1b2bk3e9A8pkCWJDfmPPFcm1hFM130_provenance
a
np:Provenance
.
dgn-np:NP847109.RAAdivqJVKhDWAqaFF1b2bk3e9A8pkCWJDfmPPFcm1hFM130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP847109.RAAdivqJVKhDWAqaFF1b2bk3e9A8pkCWJDfmPPFcm1hFM130_assertion
{
miriam-gene:367
a
ncit:C16612
.
lld:C0085280
a
ncit:C7057
.
dgn-gda:DGN5f3fa285b4fe8ac1bf38f6886c63936e
sio:SIO_000628
miriam-gene:367
,
lld:C0085280
;
a
sio:SIO_001121
.
}
dgn-np:NP847109.RAAdivqJVKhDWAqaFF1b2bk3e9A8pkCWJDfmPPFcm1hFM130_provenance
{
dgn-np:NP847109.RAAdivqJVKhDWAqaFF1b2bk3e9A8pkCWJDfmPPFcm1hFM130_assertion
dcterms:description
"[The mechanisms underlying antiandrogen withdrawal syndrome (AWS) and alternative antiandrogen therapy (AAT) effectiveness were assumed to be mutations in the androgen receptor (AR), which resulted in an altered response to antiandrogens.]. 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:19790238
;
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:NP847109.RAAdivqJVKhDWAqaFF1b2bk3e9A8pkCWJDfmPPFcm1hFM130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:38+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" .
}