@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP733125.RA2Nof5lsN3cU_5FdRI7saFWCZKdOeGU_OkdUC5fzgudY
> .
@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:NP733125.RA2Nof5lsN3cU_5FdRI7saFWCZKdOeGU_OkdUC5fzgudY130_head
{
this:
np:hasAssertion
dgn-np:NP733125.RA2Nof5lsN3cU_5FdRI7saFWCZKdOeGU_OkdUC5fzgudY130_assertion
;
np:hasProvenance
dgn-np:NP733125.RA2Nof5lsN3cU_5FdRI7saFWCZKdOeGU_OkdUC5fzgudY130_provenance
;
np:hasPublicationInfo
dgn-np:NP733125.RA2Nof5lsN3cU_5FdRI7saFWCZKdOeGU_OkdUC5fzgudY130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP733125.RA2Nof5lsN3cU_5FdRI7saFWCZKdOeGU_OkdUC5fzgudY130_assertion
a
np:Assertion
.
dgn-np:NP733125.RA2Nof5lsN3cU_5FdRI7saFWCZKdOeGU_OkdUC5fzgudY130_provenance
a
np:Provenance
.
dgn-np:NP733125.RA2Nof5lsN3cU_5FdRI7saFWCZKdOeGU_OkdUC5fzgudY130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP733125.RA2Nof5lsN3cU_5FdRI7saFWCZKdOeGU_OkdUC5fzgudY130_assertion
{
miriam-gene:60675
a
ncit:C16612
.
lld:C0271623
a
ncit:C7057
.
dgn-gda:DGN25348c554a2f3f3f5070348cdacf25f5
sio:SIO_000628
miriam-gene:60675
,
lld:C0271623
;
a
sio:SIO_001121
.
}
dgn-np:NP733125.RA2Nof5lsN3cU_5FdRI7saFWCZKdOeGU_OkdUC5fzgudY130_provenance
{
dgn-np:NP733125.RA2Nof5lsN3cU_5FdRI7saFWCZKdOeGU_OkdUC5fzgudY130_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:NP733125.RA2Nof5lsN3cU_5FdRI7saFWCZKdOeGU_OkdUC5fzgudY130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:24+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" .
}