@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP242296.RACbLqihgCjdZwt3-Ya0re5evuLLNf1JBL-e2uu73duWY
> .
@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:NP242296.RACbLqihgCjdZwt3-Ya0re5evuLLNf1JBL-e2uu73duWY130_head
{
this:
np:hasAssertion
dgn-np:NP242296.RACbLqihgCjdZwt3-Ya0re5evuLLNf1JBL-e2uu73duWY130_assertion
;
np:hasProvenance
dgn-np:NP242296.RACbLqihgCjdZwt3-Ya0re5evuLLNf1JBL-e2uu73duWY130_provenance
;
np:hasPublicationInfo
dgn-np:NP242296.RACbLqihgCjdZwt3-Ya0re5evuLLNf1JBL-e2uu73duWY130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP242296.RACbLqihgCjdZwt3-Ya0re5evuLLNf1JBL-e2uu73duWY130_assertion
a
np:Assertion
.
dgn-np:NP242296.RACbLqihgCjdZwt3-Ya0re5evuLLNf1JBL-e2uu73duWY130_provenance
a
np:Provenance
.
dgn-np:NP242296.RACbLqihgCjdZwt3-Ya0re5evuLLNf1JBL-e2uu73duWY130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP242296.RACbLqihgCjdZwt3-Ya0re5evuLLNf1JBL-e2uu73duWY130_assertion
{
miriam-gene:3814
a
ncit:C16612
.
lld:C0342544
a
ncit:C7057
.
dgn-gda:DGN835135e089106be839b2265fe83e9526
sio:SIO_000628
miriam-gene:3814
,
lld:C0342544
;
a
sio:SIO_001121
.
}
dgn-np:NP242296.RACbLqihgCjdZwt3-Ya0re5evuLLNf1JBL-e2uu73duWY130_provenance
{
dgn-np:NP242296.RACbLqihgCjdZwt3-Ya0re5evuLLNf1JBL-e2uu73duWY130_assertion
dcterms:description
"[More recently, rare activating mutations of the kisspeptin and its receptor were identified in children with idiopathic central precocious puberty, supporting the crucial role of this system in the human pubertal onset.]. 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:20816945
;
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:NP242296.RACbLqihgCjdZwt3-Ya0re5evuLLNf1JBL-e2uu73duWY130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:15+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" .
}