@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP845946.RAsIkOGGEx6ckEgE-8nkiIX5iEp19w2xcTyi9kYe_RAa0
> .
@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:NP845946.RAsIkOGGEx6ckEgE-8nkiIX5iEp19w2xcTyi9kYe_RAa0130_head
{
this:
np:hasAssertion
dgn-np:NP845946.RAsIkOGGEx6ckEgE-8nkiIX5iEp19w2xcTyi9kYe_RAa0130_assertion
;
np:hasProvenance
dgn-np:NP845946.RAsIkOGGEx6ckEgE-8nkiIX5iEp19w2xcTyi9kYe_RAa0130_provenance
;
np:hasPublicationInfo
dgn-np:NP845946.RAsIkOGGEx6ckEgE-8nkiIX5iEp19w2xcTyi9kYe_RAa0130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP845946.RAsIkOGGEx6ckEgE-8nkiIX5iEp19w2xcTyi9kYe_RAa0130_assertion
a
np:Assertion
.
dgn-np:NP845946.RAsIkOGGEx6ckEgE-8nkiIX5iEp19w2xcTyi9kYe_RAa0130_provenance
a
np:Provenance
.
dgn-np:NP845946.RAsIkOGGEx6ckEgE-8nkiIX5iEp19w2xcTyi9kYe_RAa0130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP845946.RAsIkOGGEx6ckEgE-8nkiIX5iEp19w2xcTyi9kYe_RAa0130_assertion
{
miriam-gene:551
a
ncit:C16612
.
lld:C0935572
a
ncit:C7057
.
dgn-gda:DGN42b341c1e9d5da8ea6d7f79fba437693
sio:SIO_000628
miriam-gene:551
,
lld:C0935572
;
a
sio:SIO_001121
.
}
dgn-np:NP845946.RAsIkOGGEx6ckEgE-8nkiIX5iEp19w2xcTyi9kYe_RAa0130_provenance
{
dgn-np:NP845946.RAsIkOGGEx6ckEgE-8nkiIX5iEp19w2xcTyi9kYe_RAa0130_assertion
dcterms:description
"[Specifically, MRI identification of pituitary hyperintensity in the posterior part of the sella, now considered a clear marker of neurohypophyseal functional integrity, together with the careful analysis of pituitary stalk shape and size, have provided the most striking findings contributing to the diagnosis and understanding of some forms of 'idiopathic' CDI.]. 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:22433947
;
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:NP845946.RAsIkOGGEx6ckEgE-8nkiIX5iEp19w2xcTyi9kYe_RAa0130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:37+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" .
}