@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP1393545.RAxqMDz2VhYRdDTYx392IRKoTTXfycUFrhEjCrHmC1Zpk
> .
@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/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@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/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v4.0.0/void/
> .
dgn-np:NP1393545.RAxqMDz2VhYRdDTYx392IRKoTTXfycUFrhEjCrHmC1Zpk130_head
{
this:
np:hasAssertion
dgn-np:NP1393545.RAxqMDz2VhYRdDTYx392IRKoTTXfycUFrhEjCrHmC1Zpk130_assertion
;
np:hasProvenance
dgn-np:NP1393545.RAxqMDz2VhYRdDTYx392IRKoTTXfycUFrhEjCrHmC1Zpk130_provenance
;
np:hasPublicationInfo
dgn-np:NP1393545.RAxqMDz2VhYRdDTYx392IRKoTTXfycUFrhEjCrHmC1Zpk130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP1393545.RAxqMDz2VhYRdDTYx392IRKoTTXfycUFrhEjCrHmC1Zpk130_assertion
a
np:Assertion
.
dgn-np:NP1393545.RAxqMDz2VhYRdDTYx392IRKoTTXfycUFrhEjCrHmC1Zpk130_provenance
a
np:Provenance
.
dgn-np:NP1393545.RAxqMDz2VhYRdDTYx392IRKoTTXfycUFrhEjCrHmC1Zpk130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP1393545.RAxqMDz2VhYRdDTYx392IRKoTTXfycUFrhEjCrHmC1Zpk130_assertion
{
miriam-gene:367
a
ncit:C16612
.
lld:C0039585
a
ncit:C7057
.
dgn-gda:DGNeff417ab02a772b55f015e1cae09378d
sio:SIO_000628
miriam-gene:367
,
lld:C0039585
;
a
sio:SIO_001121
.
}
dgn-np:NP1393545.RAxqMDz2VhYRdDTYx392IRKoTTXfycUFrhEjCrHmC1Zpk130_provenance
{
dgn-np:NP1393545.RAxqMDz2VhYRdDTYx392IRKoTTXfycUFrhEjCrHmC1Zpk130_assertion
dcterms:description
"[Several mutations have been described in the human androgen receptor gene including constitutional mutations in androgen insensitivity syndrome, somatic mutations in prostate cancer and triplet expansions in Kennedy's disease (Gottlieb et al.]. 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:9554754
;
prov:wasDerivedFrom
dgn-void:befree-2016
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-2016
pav:importedOn
"2016-02-19"^^
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:NP1393545.RAxqMDz2VhYRdDTYx392IRKoTTXfycUFrhEjCrHmC1Zpk130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:52:18+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:disgenetv3.0rdf
;
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
"v4.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v4.0.0" .
}