@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP530372.RAr3yA62Mx7XNeIENAgaD0P0WaWQi8VbHhklwIVAT8an4
> .
@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:NP530372.RAr3yA62Mx7XNeIENAgaD0P0WaWQi8VbHhklwIVAT8an4130_head
{
this:
np:hasAssertion
dgn-np:NP530372.RAr3yA62Mx7XNeIENAgaD0P0WaWQi8VbHhklwIVAT8an4130_assertion
;
np:hasProvenance
dgn-np:NP530372.RAr3yA62Mx7XNeIENAgaD0P0WaWQi8VbHhklwIVAT8an4130_provenance
;
np:hasPublicationInfo
dgn-np:NP530372.RAr3yA62Mx7XNeIENAgaD0P0WaWQi8VbHhklwIVAT8an4130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP530372.RAr3yA62Mx7XNeIENAgaD0P0WaWQi8VbHhklwIVAT8an4130_assertion
a
np:Assertion
.
dgn-np:NP530372.RAr3yA62Mx7XNeIENAgaD0P0WaWQi8VbHhklwIVAT8an4130_provenance
a
np:Provenance
.
dgn-np:NP530372.RAr3yA62Mx7XNeIENAgaD0P0WaWQi8VbHhklwIVAT8an4130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP530372.RAr3yA62Mx7XNeIENAgaD0P0WaWQi8VbHhklwIVAT8an4130_assertion
{
miriam-gene:6716
a
ncit:C16612
.
lld:C0238395
a
ncit:C7057
.
dgn-gda:DGN906cd88c2a1ab095d5a149519e7eb3b3
sio:SIO_000628
miriam-gene:6716
,
lld:C0238395
;
a
sio:SIO_001121
.
}
dgn-np:NP530372.RAr3yA62Mx7XNeIENAgaD0P0WaWQi8VbHhklwIVAT8an4130_provenance
{
dgn-np:NP530372.RAr3yA62Mx7XNeIENAgaD0P0WaWQi8VbHhklwIVAT8an4130_assertion
dcterms:description
"[5 alpha steroid reductase 2 (5 alpha SR2) deficiency is an autosomal recessive enzyme defect causing male pseudohermaphroditism (MPH) because of an abnormally low peripheral conversion of testosterone to dihydrotestosterone (DHT), which is required for the normal differentiation of external male genitalia.]. 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:17551467
;
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:NP530372.RAr3yA62Mx7XNeIENAgaD0P0WaWQi8VbHhklwIVAT8an4130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:20+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" .
}