@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP568247.RAvMNQm-j22dPFh9pizh0Xjp1_lEyBI_WB2IlEsi3Klf8
> .
@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/eco.owl#
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/2.0/
> .
@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/nanopublications.trig#
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/gene-disease-association.ttl#
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v2.1.0/void.ttl#
> .
dgn-np:NP568247.RAvMNQm-j22dPFh9pizh0Xjp1_lEyBI_WB2IlEsi3Klf8130_head
{
this:
np:hasAssertion
dgn-np:NP568247.RAvMNQm-j22dPFh9pizh0Xjp1_lEyBI_WB2IlEsi3Klf8130_assertion
;
np:hasProvenance
dgn-np:NP568247.RAvMNQm-j22dPFh9pizh0Xjp1_lEyBI_WB2IlEsi3Klf8130_provenance
;
np:hasPublicationInfo
dgn-np:NP568247.RAvMNQm-j22dPFh9pizh0Xjp1_lEyBI_WB2IlEsi3Klf8130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP568247.RAvMNQm-j22dPFh9pizh0Xjp1_lEyBI_WB2IlEsi3Klf8130_assertion
a
np:Assertion
.
dgn-np:NP568247.RAvMNQm-j22dPFh9pizh0Xjp1_lEyBI_WB2IlEsi3Klf8130_provenance
a
np:Provenance
.
dgn-np:NP568247.RAvMNQm-j22dPFh9pizh0Xjp1_lEyBI_WB2IlEsi3Klf8130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP568247.RAvMNQm-j22dPFh9pizh0Xjp1_lEyBI_WB2IlEsi3Klf8130_assertion
{
miriam-gene:367
a
ncit:C16612
.
lld:C0432470
a
ncit:C7057
.
dgn-gda:DGNce173a20fcf101b2d629d5c5ac07cef8
sio:SIO_000628
miriam-gene:367
,
lld:C0432470
;
a
sio:SIO_001121
.
}
dgn-np:NP568247.RAvMNQm-j22dPFh9pizh0Xjp1_lEyBI_WB2IlEsi3Klf8130_provenance
{
dgn-np:NP568247.RAvMNQm-j22dPFh9pizh0Xjp1_lEyBI_WB2IlEsi3Klf8130_assertion
dcterms:description
"[We suggest regular molecular genetic analysis of the AR gene in 46,XY females with germ cell tumour and androgen insensitivity syndrome to detect differences in the specific regions of AR gene involved in early progression toward oncogenesis of the dysgenetic gonads.]. 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:10221692
;
prov:wasDerivedFrom
dgn-void:befree-20140225
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-20140225
pav:importedOn
"2014-02-25"^^
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:NP568247.RAvMNQm-j22dPFh9pizh0Xjp1_lEyBI_WB2IlEsi3Klf8130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:42+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:disgenetrdf
;
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
"v2.1.0.0" .
dgn-void:disgenetrdf
pav:version
"v2.1.0" .
}