@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP831504.RAsPDQDdYv46WMgH6kmzr2pDx_Zd9Kx1qJg9-nMO9ipT4
> .
@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/v3.0.0/void/
> .
dgn-np:NP831504.RAsPDQDdYv46WMgH6kmzr2pDx_Zd9Kx1qJg9-nMO9ipT4130_head
{
this:
np:hasAssertion
dgn-np:NP831504.RAsPDQDdYv46WMgH6kmzr2pDx_Zd9Kx1qJg9-nMO9ipT4130_assertion
;
np:hasProvenance
dgn-np:NP831504.RAsPDQDdYv46WMgH6kmzr2pDx_Zd9Kx1qJg9-nMO9ipT4130_provenance
;
np:hasPublicationInfo
dgn-np:NP831504.RAsPDQDdYv46WMgH6kmzr2pDx_Zd9Kx1qJg9-nMO9ipT4130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP831504.RAsPDQDdYv46WMgH6kmzr2pDx_Zd9Kx1qJg9-nMO9ipT4130_assertion
a
np:Assertion
.
dgn-np:NP831504.RAsPDQDdYv46WMgH6kmzr2pDx_Zd9Kx1qJg9-nMO9ipT4130_provenance
a
np:Provenance
.
dgn-np:NP831504.RAsPDQDdYv46WMgH6kmzr2pDx_Zd9Kx1qJg9-nMO9ipT4130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP831504.RAsPDQDdYv46WMgH6kmzr2pDx_Zd9Kx1qJg9-nMO9ipT4130_assertion
{
miriam-gene:9856
a
ncit:C16612
.
lld:C0162809
a
ncit:C7057
.
dgn-gda:DGNbd24da43e4e32b1e7e74e896a8d95d14
sio:SIO_000628
miriam-gene:9856
,
lld:C0162809
;
a
sio:SIO_001121
.
}
dgn-np:NP831504.RAsPDQDdYv46WMgH6kmzr2pDx_Zd9Kx1qJg9-nMO9ipT4130_provenance
{
dgn-np:NP831504.RAsPDQDdYv46WMgH6kmzr2pDx_Zd9Kx1qJg9-nMO9ipT4130_assertion
dcterms:description
"[Taken together, these findings suggest that autosomal genes account for the majority of familial cases of KS, and that unique neuroendocrine phenotypes consistent with some GnRH neuronal migration may exist in these patients.]. 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:11297579
;
prov:wasDerivedFrom
dgn-void:befree-20150227
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-20150227
pav:importedOn
"2015-02-27"^^
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:NP831504.RAsPDQDdYv46WMgH6kmzr2pDx_Zd9Kx1qJg9-nMO9ipT4130_publicationInfo
{
this:
dcterms:created
"2015-08-25T14:46:04+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
"v3.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v3.0.0" .
}