@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP828304.RAbiEctbeMH0pKjpD18AKNycX7QRayIGptejZSuAxIWUE
> .
@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:NP828304.RAbiEctbeMH0pKjpD18AKNycX7QRayIGptejZSuAxIWUE130_head
{
this:
np:hasAssertion
dgn-np:NP828304.RAbiEctbeMH0pKjpD18AKNycX7QRayIGptejZSuAxIWUE130_assertion
;
np:hasProvenance
dgn-np:NP828304.RAbiEctbeMH0pKjpD18AKNycX7QRayIGptejZSuAxIWUE130_provenance
;
np:hasPublicationInfo
dgn-np:NP828304.RAbiEctbeMH0pKjpD18AKNycX7QRayIGptejZSuAxIWUE130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP828304.RAbiEctbeMH0pKjpD18AKNycX7QRayIGptejZSuAxIWUE130_assertion
a
np:Assertion
.
dgn-np:NP828304.RAbiEctbeMH0pKjpD18AKNycX7QRayIGptejZSuAxIWUE130_provenance
a
np:Provenance
.
dgn-np:NP828304.RAbiEctbeMH0pKjpD18AKNycX7QRayIGptejZSuAxIWUE130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP828304.RAbiEctbeMH0pKjpD18AKNycX7QRayIGptejZSuAxIWUE130_assertion
{
miriam-gene:367
a
ncit:C16612
.
lld:C0038587
a
ncit:C7057
.
dgn-gda:DGNeef50f82c98ec094ad32727957715e9a
sio:SIO_000628
miriam-gene:367
,
lld:C0038587
;
a
sio:SIO_001121
.
}
dgn-np:NP828304.RAbiEctbeMH0pKjpD18AKNycX7QRayIGptejZSuAxIWUE130_provenance
{
dgn-np:NP828304.RAbiEctbeMH0pKjpD18AKNycX7QRayIGptejZSuAxIWUE130_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:NP828304.RAbiEctbeMH0pKjpD18AKNycX7QRayIGptejZSuAxIWUE130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:27+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" .
}