@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP912942.RABzkYC6qsZzmaWhQRv_abzt6_ilfUwDOtJOaFSWMgY0I
> .
@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:NP912942.RABzkYC6qsZzmaWhQRv_abzt6_ilfUwDOtJOaFSWMgY0I130_head
{
this:
np:hasAssertion
dgn-np:NP912942.RABzkYC6qsZzmaWhQRv_abzt6_ilfUwDOtJOaFSWMgY0I130_assertion
;
np:hasProvenance
dgn-np:NP912942.RABzkYC6qsZzmaWhQRv_abzt6_ilfUwDOtJOaFSWMgY0I130_provenance
;
np:hasPublicationInfo
dgn-np:NP912942.RABzkYC6qsZzmaWhQRv_abzt6_ilfUwDOtJOaFSWMgY0I130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP912942.RABzkYC6qsZzmaWhQRv_abzt6_ilfUwDOtJOaFSWMgY0I130_assertion
a
np:Assertion
.
dgn-np:NP912942.RABzkYC6qsZzmaWhQRv_abzt6_ilfUwDOtJOaFSWMgY0I130_provenance
a
np:Provenance
.
dgn-np:NP912942.RABzkYC6qsZzmaWhQRv_abzt6_ilfUwDOtJOaFSWMgY0I130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP912942.RABzkYC6qsZzmaWhQRv_abzt6_ilfUwDOtJOaFSWMgY0I130_assertion
{
miriam-gene:367
a
ncit:C16612
.
lld:C0039585
a
ncit:C7057
.
dgn-gda:DGNbb64f4e302fcd54de509a7f6b564f013
sio:SIO_000628
miriam-gene:367
,
lld:C0039585
;
a
sio:SIO_001121
.
}
dgn-np:NP912942.RABzkYC6qsZzmaWhQRv_abzt6_ilfUwDOtJOaFSWMgY0I130_provenance
{
dgn-np:NP912942.RABzkYC6qsZzmaWhQRv_abzt6_ilfUwDOtJOaFSWMgY0I130_assertion
dcterms:description
"[Several diseases, such as androgen insensitivity syndrome (AIS), prostate cancer and spinal bulbar muscular atrophy (SBMA), have been shown to be associated with alterations in AR function due to mutations in the AR gene or dysregulation of androgen signalling.]. 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:21796517
;
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:NP912942.RABzkYC6qsZzmaWhQRv_abzt6_ilfUwDOtJOaFSWMgY0I130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:48:37+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" .
}