@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP778223.RAAO12gUx3kFSeuflwDL0NmhVrrNzf_a2awaryBlbwwDs
> .
@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:NP778223.RAAO12gUx3kFSeuflwDL0NmhVrrNzf_a2awaryBlbwwDs130_head
{
this:
np:hasAssertion
dgn-np:NP778223.RAAO12gUx3kFSeuflwDL0NmhVrrNzf_a2awaryBlbwwDs130_assertion
;
np:hasProvenance
dgn-np:NP778223.RAAO12gUx3kFSeuflwDL0NmhVrrNzf_a2awaryBlbwwDs130_provenance
;
np:hasPublicationInfo
dgn-np:NP778223.RAAO12gUx3kFSeuflwDL0NmhVrrNzf_a2awaryBlbwwDs130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP778223.RAAO12gUx3kFSeuflwDL0NmhVrrNzf_a2awaryBlbwwDs130_assertion
a
np:Assertion
.
dgn-np:NP778223.RAAO12gUx3kFSeuflwDL0NmhVrrNzf_a2awaryBlbwwDs130_provenance
a
np:Provenance
.
dgn-np:NP778223.RAAO12gUx3kFSeuflwDL0NmhVrrNzf_a2awaryBlbwwDs130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP778223.RAAO12gUx3kFSeuflwDL0NmhVrrNzf_a2awaryBlbwwDs130_assertion
{
miriam-gene:8820
a
ncit:C16612
.
lld:C0935572
a
ncit:C7057
.
dgn-gda:DGNb4ff0a380cb9376fa49554592093cfc5
sio:SIO_000628
miriam-gene:8820
,
lld:C0935572
;
a
sio:SIO_001121
.
}
dgn-np:NP778223.RAAO12gUx3kFSeuflwDL0NmhVrrNzf_a2awaryBlbwwDs130_provenance
{
dgn-np:NP778223.RAAO12gUx3kFSeuflwDL0NmhVrrNzf_a2awaryBlbwwDs130_assertion
dcterms:description
"[Abnormal posterior pituitary migration such as the ectopic posterior pituitary lobe appearing at the level of median eminence or along the pituitary stalk have been reported in idiopathic GH deficiency or in subjects with HESX1, LHX4 and SOX3 gene mutations.]. 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:19293577
;
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:NP778223.RAAO12gUx3kFSeuflwDL0NmhVrrNzf_a2awaryBlbwwDs130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:51+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" .
}