@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP475445.RAhrELM6jS2YK6DO-3hB8kr9uggSxGtR7-cVQZhBtEUVA
> .
@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:NP475445.RAhrELM6jS2YK6DO-3hB8kr9uggSxGtR7-cVQZhBtEUVA130_head
{
this:
np:hasAssertion
dgn-np:NP475445.RAhrELM6jS2YK6DO-3hB8kr9uggSxGtR7-cVQZhBtEUVA130_assertion
;
np:hasProvenance
dgn-np:NP475445.RAhrELM6jS2YK6DO-3hB8kr9uggSxGtR7-cVQZhBtEUVA130_provenance
;
np:hasPublicationInfo
dgn-np:NP475445.RAhrELM6jS2YK6DO-3hB8kr9uggSxGtR7-cVQZhBtEUVA130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP475445.RAhrELM6jS2YK6DO-3hB8kr9uggSxGtR7-cVQZhBtEUVA130_assertion
a
np:Assertion
.
dgn-np:NP475445.RAhrELM6jS2YK6DO-3hB8kr9uggSxGtR7-cVQZhBtEUVA130_provenance
a
np:Provenance
.
dgn-np:NP475445.RAhrELM6jS2YK6DO-3hB8kr9uggSxGtR7-cVQZhBtEUVA130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP475445.RAhrELM6jS2YK6DO-3hB8kr9uggSxGtR7-cVQZhBtEUVA130_assertion
{
miriam-gene:3973
a
ncit:C16612
.
lld:C1504412
a
ncit:C7057
.
dgn-gda:DGN529167938df9cf6d7c07eca870631bfe
sio:SIO_000628
miriam-gene:3973
,
lld:C1504412
;
a
sio:SIO_001121
.
}
dgn-np:NP475445.RAhrELM6jS2YK6DO-3hB8kr9uggSxGtR7-cVQZhBtEUVA130_provenance
{
dgn-np:NP475445.RAhrELM6jS2YK6DO-3hB8kr9uggSxGtR7-cVQZhBtEUVA130_assertion
dcterms:description
"[Testotoxicosis is a form of precocious puberty in which the Leydig cells secrete testosterone in the absence of luteinizing hormone, often due to constitutive activation of the luteinizing hormone receptor and (indirectly) Gs (refs 1-4).]. 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:8072545
;
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:NP475445.RAhrELM6jS2YK6DO-3hB8kr9uggSxGtR7-cVQZhBtEUVA130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:45+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" .
}