@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP1384985.RAp759oUV0qPcDYiYepWnd-f13eRm9cEYtJ4w0HHXDpbY
> .
@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:NP1384985.RAp759oUV0qPcDYiYepWnd-f13eRm9cEYtJ4w0HHXDpbY130_head
{
this:
np:hasAssertion
dgn-np:NP1384985.RAp759oUV0qPcDYiYepWnd-f13eRm9cEYtJ4w0HHXDpbY130_assertion
;
np:hasProvenance
dgn-np:NP1384985.RAp759oUV0qPcDYiYepWnd-f13eRm9cEYtJ4w0HHXDpbY130_provenance
;
np:hasPublicationInfo
dgn-np:NP1384985.RAp759oUV0qPcDYiYepWnd-f13eRm9cEYtJ4w0HHXDpbY130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP1384985.RAp759oUV0qPcDYiYepWnd-f13eRm9cEYtJ4w0HHXDpbY130_assertion
a
np:Assertion
.
dgn-np:NP1384985.RAp759oUV0qPcDYiYepWnd-f13eRm9cEYtJ4w0HHXDpbY130_provenance
a
np:Provenance
.
dgn-np:NP1384985.RAp759oUV0qPcDYiYepWnd-f13eRm9cEYtJ4w0HHXDpbY130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP1384985.RAp759oUV0qPcDYiYepWnd-f13eRm9cEYtJ4w0HHXDpbY130_assertion
{
miriam-gene:5449
a
ncit:C16612
.
lld:C0020635
a
ncit:C7057
.
dgn-gda:DGN6b308551d66981472a9cb258915f129d
sio:SIO_000628
miriam-gene:5449
,
lld:C0020635
;
a
sio:SIO_001121
.
}
dgn-np:NP1384985.RAp759oUV0qPcDYiYepWnd-f13eRm9cEYtJ4w0HHXDpbY130_provenance
{
dgn-np:NP1384985.RAp759oUV0qPcDYiYepWnd-f13eRm9cEYtJ4w0HHXDpbY130_assertion
dcterms:description
"[Diagnosing Pit-1 gene mutations as a rare cause of combined pituitary deficiency is important both for genetic counselling as well as for predicting the future course in the patient (spontaneous puberty, no glucocorticoid substitution necessary during stress periods).]. 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:9392393
;
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:NP1384985.RAp759oUV0qPcDYiYepWnd-f13eRm9cEYtJ4w0HHXDpbY130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:52:14+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" .
}