@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP501311.RAjVlQzSxrplDjnqEn0ZjC6DfnIEbk6xh1GV8VVXCo6tg
> .
@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:NP501311.RAjVlQzSxrplDjnqEn0ZjC6DfnIEbk6xh1GV8VVXCo6tg130_head
{
this:
np:hasAssertion
dgn-np:NP501311.RAjVlQzSxrplDjnqEn0ZjC6DfnIEbk6xh1GV8VVXCo6tg130_assertion
;
np:hasProvenance
dgn-np:NP501311.RAjVlQzSxrplDjnqEn0ZjC6DfnIEbk6xh1GV8VVXCo6tg130_provenance
;
np:hasPublicationInfo
dgn-np:NP501311.RAjVlQzSxrplDjnqEn0ZjC6DfnIEbk6xh1GV8VVXCo6tg130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP501311.RAjVlQzSxrplDjnqEn0ZjC6DfnIEbk6xh1GV8VVXCo6tg130_assertion
a
np:Assertion
.
dgn-np:NP501311.RAjVlQzSxrplDjnqEn0ZjC6DfnIEbk6xh1GV8VVXCo6tg130_provenance
a
np:Provenance
.
dgn-np:NP501311.RAjVlQzSxrplDjnqEn0ZjC6DfnIEbk6xh1GV8VVXCo6tg130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP501311.RAjVlQzSxrplDjnqEn0ZjC6DfnIEbk6xh1GV8VVXCo6tg130_assertion
{
miriam-gene:3973
a
ncit:C16612
.
lld:C0034013
a
ncit:C7057
.
dgn-gda:DGN92149f4c7b1d2edeaa33b7ba016b8044
sio:SIO_000628
miriam-gene:3973
,
lld:C0034013
;
a
sio:SIO_001121
.
}
dgn-np:NP501311.RAjVlQzSxrplDjnqEn0ZjC6DfnIEbk6xh1GV8VVXCo6tg130_provenance
{
dgn-np:NP501311.RAjVlQzSxrplDjnqEn0ZjC6DfnIEbk6xh1GV8VVXCo6tg130_assertion
dcterms:description
"[Previous studies by others have shown that some forms of familial male precocious puberty are associated with mutations of the human LHR in the sixth transmembrane region that result in constitutive activation of the receptor.]. 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:9169417
;
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:NP501311.RAjVlQzSxrplDjnqEn0ZjC6DfnIEbk6xh1GV8VVXCo6tg130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:59+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" .
}