@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP223492.RAcxtUYMQg7H4aK1yn_ObDWmCN7a9q5KkweUAtMoOXrdw
> .
@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:NP223492.RAcxtUYMQg7H4aK1yn_ObDWmCN7a9q5KkweUAtMoOXrdw130_head
{
this:
np:hasAssertion
dgn-np:NP223492.RAcxtUYMQg7H4aK1yn_ObDWmCN7a9q5KkweUAtMoOXrdw130_assertion
;
np:hasProvenance
dgn-np:NP223492.RAcxtUYMQg7H4aK1yn_ObDWmCN7a9q5KkweUAtMoOXrdw130_provenance
;
np:hasPublicationInfo
dgn-np:NP223492.RAcxtUYMQg7H4aK1yn_ObDWmCN7a9q5KkweUAtMoOXrdw130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP223492.RAcxtUYMQg7H4aK1yn_ObDWmCN7a9q5KkweUAtMoOXrdw130_assertion
a
np:Assertion
.
dgn-np:NP223492.RAcxtUYMQg7H4aK1yn_ObDWmCN7a9q5KkweUAtMoOXrdw130_provenance
a
np:Provenance
.
dgn-np:NP223492.RAcxtUYMQg7H4aK1yn_ObDWmCN7a9q5KkweUAtMoOXrdw130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP223492.RAcxtUYMQg7H4aK1yn_ObDWmCN7a9q5KkweUAtMoOXrdw130_assertion
{
miriam-gene:10046
a
ncit:C16612
.
lld:C0341787
a
ncit:C7057
.
dgn-gda:DGNc74b4d5011a6280988f6e88697b4777e
sio:SIO_000628
miriam-gene:10046
,
lld:C0341787
;
a
sio:SIO_001121
.
}
dgn-np:NP223492.RAcxtUYMQg7H4aK1yn_ObDWmCN7a9q5KkweUAtMoOXrdw130_provenance
{
dgn-np:NP223492.RAcxtUYMQg7H4aK1yn_ObDWmCN7a9q5KkweUAtMoOXrdw130_assertion
dcterms:description
"[Mutations in chromosome X open reading frame 6 (CXorf6), a recently described candidate gene involved in the development of male genitalia, have been found in patients with complex 46,XY disorders of sexual development (46,XY DSD) including micropenis, bifid scrotum, and penoscrotal hypospadias.]. 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:18635673
;
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:NP223492.RAcxtUYMQg7H4aK1yn_ObDWmCN7a9q5KkweUAtMoOXrdw130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:04+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" .
}