@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP388352.RAdXoespRwYN5Yty7qa1qnk5ce4VmVGwqOfF3yB679F-c
> .
@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:NP388352.RAdXoespRwYN5Yty7qa1qnk5ce4VmVGwqOfF3yB679F-c130_head
{
this:
np:hasAssertion
dgn-np:NP388352.RAdXoespRwYN5Yty7qa1qnk5ce4VmVGwqOfF3yB679F-c130_assertion
;
np:hasProvenance
dgn-np:NP388352.RAdXoespRwYN5Yty7qa1qnk5ce4VmVGwqOfF3yB679F-c130_provenance
;
np:hasPublicationInfo
dgn-np:NP388352.RAdXoespRwYN5Yty7qa1qnk5ce4VmVGwqOfF3yB679F-c130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP388352.RAdXoespRwYN5Yty7qa1qnk5ce4VmVGwqOfF3yB679F-c130_assertion
a
np:Assertion
.
dgn-np:NP388352.RAdXoespRwYN5Yty7qa1qnk5ce4VmVGwqOfF3yB679F-c130_provenance
a
np:Provenance
.
dgn-np:NP388352.RAdXoespRwYN5Yty7qa1qnk5ce4VmVGwqOfF3yB679F-c130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP388352.RAdXoespRwYN5Yty7qa1qnk5ce4VmVGwqOfF3yB679F-c130_assertion
{
miriam-gene:5443
a
ncit:C16612
.
lld:C0221406
a
ncit:C7057
.
dgn-gda:DGN89b2875f6905cc53c814719ea496cb8a
sio:SIO_000628
miriam-gene:5443
,
lld:C0221406
;
a
sio:SIO_001121
.
}
dgn-np:NP388352.RAdXoespRwYN5Yty7qa1qnk5ce4VmVGwqOfF3yB679F-c130_provenance
{
dgn-np:NP388352.RAdXoespRwYN5Yty7qa1qnk5ce4VmVGwqOfF3yB679F-c130_assertion
dcterms:description
"[In order to analyse the presence of different POMC transcripts, we extracted total RNA from peripheral lymphocytes of 10 patients with Cushing's disease, 10 with ectopic Cushing syndrome, and 20 controls as well as from pituitary tissues (2 ACTH-omas and a normal pituitary polyA+ sample).]. 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:18075284
;
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:NP388352.RAdXoespRwYN5Yty7qa1qnk5ce4VmVGwqOfF3yB679F-c130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:51+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" .
}