@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP599566.RAIcLQNZVUtnhQCIIaPUPa-Mdlp9kWZPRxBpNl1hdbzVQ
> .
@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:NP599566.RAIcLQNZVUtnhQCIIaPUPa-Mdlp9kWZPRxBpNl1hdbzVQ130_head
{
this:
np:hasAssertion
dgn-np:NP599566.RAIcLQNZVUtnhQCIIaPUPa-Mdlp9kWZPRxBpNl1hdbzVQ130_assertion
;
np:hasProvenance
dgn-np:NP599566.RAIcLQNZVUtnhQCIIaPUPa-Mdlp9kWZPRxBpNl1hdbzVQ130_provenance
;
np:hasPublicationInfo
dgn-np:NP599566.RAIcLQNZVUtnhQCIIaPUPa-Mdlp9kWZPRxBpNl1hdbzVQ130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP599566.RAIcLQNZVUtnhQCIIaPUPa-Mdlp9kWZPRxBpNl1hdbzVQ130_assertion
a
np:Assertion
.
dgn-np:NP599566.RAIcLQNZVUtnhQCIIaPUPa-Mdlp9kWZPRxBpNl1hdbzVQ130_provenance
a
np:Provenance
.
dgn-np:NP599566.RAIcLQNZVUtnhQCIIaPUPa-Mdlp9kWZPRxBpNl1hdbzVQ130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP599566.RAIcLQNZVUtnhQCIIaPUPa-Mdlp9kWZPRxBpNl1hdbzVQ130_assertion
{
miriam-gene:960
a
ncit:C16612
.
lld:C0034013
a
ncit:C7057
.
dgn-gda:DGN92a024c93bdc6e816cb354348e2cdda7
sio:SIO_000628
miriam-gene:960
,
lld:C0034013
;
a
sio:SIO_001121
.
}
dgn-np:NP599566.RAIcLQNZVUtnhQCIIaPUPa-Mdlp9kWZPRxBpNl1hdbzVQ130_provenance
{
dgn-np:NP599566.RAIcLQNZVUtnhQCIIaPUPa-Mdlp9kWZPRxBpNl1hdbzVQ130_assertion
dcterms:description
"[It is suggested that this mutation caused constitutive activation of the LHR, which results in excessive formation of androgens in Leydig cells and is responsible for the symptoms of precocious puberty in this patient.]. 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:11200941
;
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:NP599566.RAIcLQNZVUtnhQCIIaPUPa-Mdlp9kWZPRxBpNl1hdbzVQ130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:00+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" .
}