@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP264320.RABExRoA8cv5yIwWgGS2f0c8TD2ZoF_ordNDAlYsBU8U8
> .
@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:NP264320.RABExRoA8cv5yIwWgGS2f0c8TD2ZoF_ordNDAlYsBU8U8130_head
{
this:
np:hasAssertion
dgn-np:NP264320.RABExRoA8cv5yIwWgGS2f0c8TD2ZoF_ordNDAlYsBU8U8130_assertion
;
np:hasProvenance
dgn-np:NP264320.RABExRoA8cv5yIwWgGS2f0c8TD2ZoF_ordNDAlYsBU8U8130_provenance
;
np:hasPublicationInfo
dgn-np:NP264320.RABExRoA8cv5yIwWgGS2f0c8TD2ZoF_ordNDAlYsBU8U8130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP264320.RABExRoA8cv5yIwWgGS2f0c8TD2ZoF_ordNDAlYsBU8U8130_assertion
a
np:Assertion
.
dgn-np:NP264320.RABExRoA8cv5yIwWgGS2f0c8TD2ZoF_ordNDAlYsBU8U8130_provenance
a
np:Provenance
.
dgn-np:NP264320.RABExRoA8cv5yIwWgGS2f0c8TD2ZoF_ordNDAlYsBU8U8130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP264320.RABExRoA8cv5yIwWgGS2f0c8TD2ZoF_ordNDAlYsBU8U8130_assertion
{
miriam-gene:367
a
ncit:C16612
.
lld:C0039585
a
ncit:C7057
.
dgn-gda:DGNc8110056639659ae83c22a8f6a451872
sio:SIO_000628
miriam-gene:367
,
lld:C0039585
;
a
sio:SIO_001121
.
}
dgn-np:NP264320.RABExRoA8cv5yIwWgGS2f0c8TD2ZoF_ordNDAlYsBU8U8130_provenance
{
dgn-np:NP264320.RABExRoA8cv5yIwWgGS2f0c8TD2ZoF_ordNDAlYsBU8U8130_assertion
dcterms:description
"[Mutations of the androgen receptor gene causing androgen insensitivity syndrome in 46, XY individuals, result in phenotypes ranging from complete female to ambiguous genitalia to males with minor degrees of undervirilization.]. 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:10502786
;
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:NP264320.RABExRoA8cv5yIwWgGS2f0c8TD2ZoF_ordNDAlYsBU8U8130_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" .
}