@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP710720.RAdModSgVcyae6snvRq4f2sk8WjIGf9gaINB9o0Jbwt-o
> .
@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:NP710720.RAdModSgVcyae6snvRq4f2sk8WjIGf9gaINB9o0Jbwt-o130_head
{
this:
np:hasAssertion
dgn-np:NP710720.RAdModSgVcyae6snvRq4f2sk8WjIGf9gaINB9o0Jbwt-o130_assertion
;
np:hasProvenance
dgn-np:NP710720.RAdModSgVcyae6snvRq4f2sk8WjIGf9gaINB9o0Jbwt-o130_provenance
;
np:hasPublicationInfo
dgn-np:NP710720.RAdModSgVcyae6snvRq4f2sk8WjIGf9gaINB9o0Jbwt-o130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP710720.RAdModSgVcyae6snvRq4f2sk8WjIGf9gaINB9o0Jbwt-o130_assertion
a
np:Assertion
.
dgn-np:NP710720.RAdModSgVcyae6snvRq4f2sk8WjIGf9gaINB9o0Jbwt-o130_provenance
a
np:Provenance
.
dgn-np:NP710720.RAdModSgVcyae6snvRq4f2sk8WjIGf9gaINB9o0Jbwt-o130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP710720.RAdModSgVcyae6snvRq4f2sk8WjIGf9gaINB9o0Jbwt-o130_assertion
{
miriam-gene:367
a
ncit:C16612
.
lld:C0008626
a
ncit:C7057
.
dgn-gda:DGNbe5ed7527d98089107a2257d5846dfe5
sio:SIO_000628
miriam-gene:367
,
lld:C0008626
;
a
sio:SIO_001121
.
}
dgn-np:NP710720.RAdModSgVcyae6snvRq4f2sk8WjIGf9gaINB9o0Jbwt-o130_provenance
{
dgn-np:NP710720.RAdModSgVcyae6snvRq4f2sk8WjIGf9gaINB9o0Jbwt-o130_assertion
dcterms:description
"[The analysis of the chromosomal abnormality suggests that this translocation may remove one or more upstream regulatory elements of the AR gene that are essential for its normal expression and its role in typical external masculinization.]. 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:15452386
;
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:NP710720.RAdModSgVcyae6snvRq4f2sk8WjIGf9gaINB9o0Jbwt-o130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:12+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" .
}