@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP302825.RANQjKhWUWCCVWwIhg4S9RHJQLcxELixObW9aaT4zfL0A
> .
@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:NP302825.RANQjKhWUWCCVWwIhg4S9RHJQLcxELixObW9aaT4zfL0A130_head
{
this:
np:hasAssertion
dgn-np:NP302825.RANQjKhWUWCCVWwIhg4S9RHJQLcxELixObW9aaT4zfL0A130_assertion
;
np:hasProvenance
dgn-np:NP302825.RANQjKhWUWCCVWwIhg4S9RHJQLcxELixObW9aaT4zfL0A130_provenance
;
np:hasPublicationInfo
dgn-np:NP302825.RANQjKhWUWCCVWwIhg4S9RHJQLcxELixObW9aaT4zfL0A130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP302825.RANQjKhWUWCCVWwIhg4S9RHJQLcxELixObW9aaT4zfL0A130_assertion
a
np:Assertion
.
dgn-np:NP302825.RANQjKhWUWCCVWwIhg4S9RHJQLcxELixObW9aaT4zfL0A130_provenance
a
np:Provenance
.
dgn-np:NP302825.RANQjKhWUWCCVWwIhg4S9RHJQLcxELixObW9aaT4zfL0A130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP302825.RANQjKhWUWCCVWwIhg4S9RHJQLcxELixObW9aaT4zfL0A130_assertion
{
miriam-gene:3814
a
ncit:C16612
.
lld:C0342543
a
ncit:C7057
.
dgn-gda:DGN5756854ee782364155886e19b98d02cb
sio:SIO_000628
miriam-gene:3814
,
lld:C0342543
;
a
sio:SIO_001121
.
}
dgn-np:NP302825.RANQjKhWUWCCVWwIhg4S9RHJQLcxELixObW9aaT4zfL0A130_provenance
{
dgn-np:NP302825.RANQjKhWUWCCVWwIhg4S9RHJQLcxELixObW9aaT4zfL0A130_assertion
dcterms:description
"[Interestingly, rare gain-of-function mutations of the genes encoding the kisspeptin and its receptor were recently associated with central precocious puberty phenotype, indicating that the premature activation of the reproductive axis may be also caused by genetic mutations.]. 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:20188792
;
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:NP302825.RANQjKhWUWCCVWwIhg4S9RHJQLcxELixObW9aaT4zfL0A130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:54+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" .
}