@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP253792.RAGxdtw5oqghsF6QYQ4Tze4AD7KM_jiBjqv5tqid8FrsI
> .
@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:NP253792.RAGxdtw5oqghsF6QYQ4Tze4AD7KM_jiBjqv5tqid8FrsI130_head
{
this:
np:hasAssertion
dgn-np:NP253792.RAGxdtw5oqghsF6QYQ4Tze4AD7KM_jiBjqv5tqid8FrsI130_assertion
;
np:hasProvenance
dgn-np:NP253792.RAGxdtw5oqghsF6QYQ4Tze4AD7KM_jiBjqv5tqid8FrsI130_provenance
;
np:hasPublicationInfo
dgn-np:NP253792.RAGxdtw5oqghsF6QYQ4Tze4AD7KM_jiBjqv5tqid8FrsI130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP253792.RAGxdtw5oqghsF6QYQ4Tze4AD7KM_jiBjqv5tqid8FrsI130_assertion
a
np:Assertion
.
dgn-np:NP253792.RAGxdtw5oqghsF6QYQ4Tze4AD7KM_jiBjqv5tqid8FrsI130_provenance
a
np:Provenance
.
dgn-np:NP253792.RAGxdtw5oqghsF6QYQ4Tze4AD7KM_jiBjqv5tqid8FrsI130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP253792.RAGxdtw5oqghsF6QYQ4Tze4AD7KM_jiBjqv5tqid8FrsI130_assertion
{
miriam-gene:2516
a
ncit:C16612
.
lld:C0041408
a
ncit:C7057
.
dgn-gda:DGN440c2fc947fb082195735b0df3e57491
sio:SIO_000628
miriam-gene:2516
,
lld:C0041408
;
a
sio:SIO_001121
.
}
dgn-np:NP253792.RAGxdtw5oqghsF6QYQ4Tze4AD7KM_jiBjqv5tqid8FrsI130_provenance
{
dgn-np:NP253792.RAGxdtw5oqghsF6QYQ4Tze4AD7KM_jiBjqv5tqid8FrsI130_assertion
dcterms:description
"[NR5A1 mutations have been identified in patients with various forms of 46,XY disorders of sex development (DSD), including complete gonadal dysgenesis with or without adrenal insufficiency, mild testicular dysgenesis with ambiguous external genitalia or female external genitalia with clitoromegaly, 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:21654157
;
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:NP253792.RAGxdtw5oqghsF6QYQ4Tze4AD7KM_jiBjqv5tqid8FrsI130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:22+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" .
}