@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP262890.RANHjAeHLkHRS6p8v7EVNHsn-xf1O11xWmPRve_dupmMc
> .
@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:NP262890.RANHjAeHLkHRS6p8v7EVNHsn-xf1O11xWmPRve_dupmMc130_head
{
this:
np:hasAssertion
dgn-np:NP262890.RANHjAeHLkHRS6p8v7EVNHsn-xf1O11xWmPRve_dupmMc130_assertion
;
np:hasProvenance
dgn-np:NP262890.RANHjAeHLkHRS6p8v7EVNHsn-xf1O11xWmPRve_dupmMc130_provenance
;
np:hasPublicationInfo
dgn-np:NP262890.RANHjAeHLkHRS6p8v7EVNHsn-xf1O11xWmPRve_dupmMc130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP262890.RANHjAeHLkHRS6p8v7EVNHsn-xf1O11xWmPRve_dupmMc130_assertion
a
np:Assertion
.
dgn-np:NP262890.RANHjAeHLkHRS6p8v7EVNHsn-xf1O11xWmPRve_dupmMc130_provenance
a
np:Provenance
.
dgn-np:NP262890.RANHjAeHLkHRS6p8v7EVNHsn-xf1O11xWmPRve_dupmMc130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP262890.RANHjAeHLkHRS6p8v7EVNHsn-xf1O11xWmPRve_dupmMc130_assertion
{
miriam-gene:367
a
ncit:C16612
.
lld:C0039585
a
ncit:C7057
.
dgn-gda:DGN167da1204ecbc5f100c00224fc8aa0e7
sio:SIO_000628
miriam-gene:367
,
lld:C0039585
;
a
sio:SIO_001121
.
}
dgn-np:NP262890.RANHjAeHLkHRS6p8v7EVNHsn-xf1O11xWmPRve_dupmMc130_provenance
{
dgn-np:NP262890.RANHjAeHLkHRS6p8v7EVNHsn-xf1O11xWmPRve_dupmMc130_assertion
dcterms:description
"[Recently, we demonstrated a previously unknown high rate of de novo mutations of the androgen receptor (AR) gene in androgen insensitivity syndrome (AIS) with some resulting in somatic mosaicism of mutant and wild type AR alleles.]. 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:10485299
;
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:NP262890.RANHjAeHLkHRS6p8v7EVNHsn-xf1O11xWmPRve_dupmMc130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:43:45+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" .
}