@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP814669.RAkWsq2MwCFOZdke1_XqvW_jRhpe8S-gPcF281KXxAm_w
> .
@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/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@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/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v4.0.0/void/
> .
dgn-np:NP814669.RAkWsq2MwCFOZdke1_XqvW_jRhpe8S-gPcF281KXxAm_w130_head
{
this:
np:hasAssertion
dgn-np:NP814669.RAkWsq2MwCFOZdke1_XqvW_jRhpe8S-gPcF281KXxAm_w130_assertion
;
np:hasProvenance
dgn-np:NP814669.RAkWsq2MwCFOZdke1_XqvW_jRhpe8S-gPcF281KXxAm_w130_provenance
;
np:hasPublicationInfo
dgn-np:NP814669.RAkWsq2MwCFOZdke1_XqvW_jRhpe8S-gPcF281KXxAm_w130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP814669.RAkWsq2MwCFOZdke1_XqvW_jRhpe8S-gPcF281KXxAm_w130_assertion
a
np:Assertion
.
dgn-np:NP814669.RAkWsq2MwCFOZdke1_XqvW_jRhpe8S-gPcF281KXxAm_w130_provenance
a
np:Provenance
.
dgn-np:NP814669.RAkWsq2MwCFOZdke1_XqvW_jRhpe8S-gPcF281KXxAm_w130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP814669.RAkWsq2MwCFOZdke1_XqvW_jRhpe8S-gPcF281KXxAm_w130_assertion
{
miriam-gene:128674
a
ncit:C16612
.
lld:C0271623
a
ncit:C7057
.
dgn-gda:DGN1f6db122e45a005418fc8bc5ef4dc4e7
sio:SIO_000628
miriam-gene:128674
,
lld:C0271623
;
a
sio:SIO_001121
.
}
dgn-np:NP814669.RAkWsq2MwCFOZdke1_XqvW_jRhpe8S-gPcF281KXxAm_w130_provenance
{
dgn-np:NP814669.RAkWsq2MwCFOZdke1_XqvW_jRhpe8S-gPcF281KXxAm_w130_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-2016
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-2016
pav:importedOn
"2016-02-19"^^
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:NP814669.RAkWsq2MwCFOZdke1_XqvW_jRhpe8S-gPcF281KXxAm_w130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:47:54+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:disgenetv3.0rdf
;
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
"v4.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v4.0.0" .
}