@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP529131.RATtqCXUGy1zNAEAaXgmdelt-KuHwQ9Ia68mlb9DXF40I
> .
@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:NP529131.RATtqCXUGy1zNAEAaXgmdelt-KuHwQ9Ia68mlb9DXF40I130_head
{
this:
np:hasAssertion
dgn-np:NP529131.RATtqCXUGy1zNAEAaXgmdelt-KuHwQ9Ia68mlb9DXF40I130_assertion
;
np:hasProvenance
dgn-np:NP529131.RATtqCXUGy1zNAEAaXgmdelt-KuHwQ9Ia68mlb9DXF40I130_provenance
;
np:hasPublicationInfo
dgn-np:NP529131.RATtqCXUGy1zNAEAaXgmdelt-KuHwQ9Ia68mlb9DXF40I130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP529131.RATtqCXUGy1zNAEAaXgmdelt-KuHwQ9Ia68mlb9DXF40I130_assertion
a
np:Assertion
.
dgn-np:NP529131.RATtqCXUGy1zNAEAaXgmdelt-KuHwQ9Ia68mlb9DXF40I130_provenance
a
np:Provenance
.
dgn-np:NP529131.RATtqCXUGy1zNAEAaXgmdelt-KuHwQ9Ia68mlb9DXF40I130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP529131.RATtqCXUGy1zNAEAaXgmdelt-KuHwQ9Ia68mlb9DXF40I130_assertion
{
miriam-gene:367
a
ncit:C16612
.
lld:C0752353
a
ncit:C7057
.
dgn-gda:DGNb6e113d4dd4ed93f98b3712bee602ae4
sio:SIO_000628
miriam-gene:367
,
lld:C0752353
;
a
sio:SIO_001121
.
}
dgn-np:NP529131.RATtqCXUGy1zNAEAaXgmdelt-KuHwQ9Ia68mlb9DXF40I130_provenance
{
dgn-np:NP529131.RATtqCXUGy1zNAEAaXgmdelt-KuHwQ9Ia68mlb9DXF40I130_assertion
dcterms:description
"[This review summarizes the most recent information on two pathologies linked to mutations of the androgen receptor, namely, the complete androgen insensitivity syndrome (CAIS) and the spinal and bulbar muscular atrophy (SBMA or Kennedy's disease).]. 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:16388114
;
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:NP529131.RATtqCXUGy1zNAEAaXgmdelt-KuHwQ9Ia68mlb9DXF40I130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:45:44+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" .
}