@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP601827.RA0NUyMXTLnKD50tkWSItsnnvLWw38PMZdVWbE3wHcGjM
> .
@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:NP601827.RA0NUyMXTLnKD50tkWSItsnnvLWw38PMZdVWbE3wHcGjM130_head
{
this:
np:hasAssertion
dgn-np:NP601827.RA0NUyMXTLnKD50tkWSItsnnvLWw38PMZdVWbE3wHcGjM130_assertion
;
np:hasProvenance
dgn-np:NP601827.RA0NUyMXTLnKD50tkWSItsnnvLWw38PMZdVWbE3wHcGjM130_provenance
;
np:hasPublicationInfo
dgn-np:NP601827.RA0NUyMXTLnKD50tkWSItsnnvLWw38PMZdVWbE3wHcGjM130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP601827.RA0NUyMXTLnKD50tkWSItsnnvLWw38PMZdVWbE3wHcGjM130_assertion
a
np:Assertion
.
dgn-np:NP601827.RA0NUyMXTLnKD50tkWSItsnnvLWw38PMZdVWbE3wHcGjM130_provenance
a
np:Provenance
.
dgn-np:NP601827.RA0NUyMXTLnKD50tkWSItsnnvLWw38PMZdVWbE3wHcGjM130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP601827.RA0NUyMXTLnKD50tkWSItsnnvLWw38PMZdVWbE3wHcGjM130_assertion
{
miriam-gene:128674
a
ncit:C16612
.
lld:C0022735
a
ncit:C7057
.
dgn-gda:DGNd237e584f89207eb757c4bcd80bf3e36
sio:SIO_000628
miriam-gene:128674
,
lld:C0022735
;
a
sio:SIO_001121
.
}
dgn-np:NP601827.RA0NUyMXTLnKD50tkWSItsnnvLWw38PMZdVWbE3wHcGjM130_provenance
{
dgn-np:NP601827.RA0NUyMXTLnKD50tkWSItsnnvLWw38PMZdVWbE3wHcGjM130_assertion
dcterms:description
"[Indeed, the evidence from several naturally inactivating mutations in the PROK2 and PROKR2 genes in patients with Kallmann syndrome and normosmic hypogonadotropic hypogonadism also indicate the essential role of PROK2 in olfactory bulb morphogenesis and GnRH secretion in humans.]. 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:20502053
;
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:NP601827.RA0NUyMXTLnKD50tkWSItsnnvLWw38PMZdVWbE3wHcGjM130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:01+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" .
}