@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP868817.RAzlFjc1IrfUZpwiJncQeJjDzTrNi54wDLY9eI7Pln7pM
> .
@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:NP868817.RAzlFjc1IrfUZpwiJncQeJjDzTrNi54wDLY9eI7Pln7pM130_head
{
this:
np:hasAssertion
dgn-np:NP868817.RAzlFjc1IrfUZpwiJncQeJjDzTrNi54wDLY9eI7Pln7pM130_assertion
;
np:hasProvenance
dgn-np:NP868817.RAzlFjc1IrfUZpwiJncQeJjDzTrNi54wDLY9eI7Pln7pM130_provenance
;
np:hasPublicationInfo
dgn-np:NP868817.RAzlFjc1IrfUZpwiJncQeJjDzTrNi54wDLY9eI7Pln7pM130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP868817.RAzlFjc1IrfUZpwiJncQeJjDzTrNi54wDLY9eI7Pln7pM130_assertion
a
np:Assertion
.
dgn-np:NP868817.RAzlFjc1IrfUZpwiJncQeJjDzTrNi54wDLY9eI7Pln7pM130_provenance
a
np:Provenance
.
dgn-np:NP868817.RAzlFjc1IrfUZpwiJncQeJjDzTrNi54wDLY9eI7Pln7pM130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP868817.RAzlFjc1IrfUZpwiJncQeJjDzTrNi54wDLY9eI7Pln7pM130_assertion
{
miriam-gene:5015
a
ncit:C16612
.
lld:C0020635
a
ncit:C7057
.
dgn-gda:DGNdfb8f70e393a4b2b0bb02bd7e9d24335
sio:SIO_000628
miriam-gene:5015
,
lld:C0020635
;
a
sio:SIO_001121
.
}
dgn-np:NP868817.RAzlFjc1IrfUZpwiJncQeJjDzTrNi54wDLY9eI7Pln7pM130_provenance
{
dgn-np:NP868817.RAzlFjc1IrfUZpwiJncQeJjDzTrNi54wDLY9eI7Pln7pM130_assertion
dcterms:description
"[PROK2 and PROKR2 and all genes previously known to be involved in hypopituitarism with pituitary stalk interruption (LHX4, HESX1, OTX2, and SOX3) were screened in 72 index cases with pituitary stalk interruption syndrome from the GENHYPOPIT database.]. 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:22466334
;
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:NP868817.RAzlFjc1IrfUZpwiJncQeJjDzTrNi54wDLY9eI7Pln7pM130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:51+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" .
}