@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP562192.RA_o9xK2pCpqrVPv4eYn9umMd_Nt2pELOhJQSXNWgQh84
> .
@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:NP562192.RA_o9xK2pCpqrVPv4eYn9umMd_Nt2pELOhJQSXNWgQh84130_head
{
this:
np:hasAssertion
dgn-np:NP562192.RA_o9xK2pCpqrVPv4eYn9umMd_Nt2pELOhJQSXNWgQh84130_assertion
;
np:hasProvenance
dgn-np:NP562192.RA_o9xK2pCpqrVPv4eYn9umMd_Nt2pELOhJQSXNWgQh84130_provenance
;
np:hasPublicationInfo
dgn-np:NP562192.RA_o9xK2pCpqrVPv4eYn9umMd_Nt2pELOhJQSXNWgQh84130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP562192.RA_o9xK2pCpqrVPv4eYn9umMd_Nt2pELOhJQSXNWgQh84130_assertion
a
np:Assertion
.
dgn-np:NP562192.RA_o9xK2pCpqrVPv4eYn9umMd_Nt2pELOhJQSXNWgQh84130_provenance
a
np:Provenance
.
dgn-np:NP562192.RA_o9xK2pCpqrVPv4eYn9umMd_Nt2pELOhJQSXNWgQh84130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP562192.RA_o9xK2pCpqrVPv4eYn9umMd_Nt2pELOhJQSXNWgQh84130_assertion
{
miriam-gene:5443
a
ncit:C16612
.
lld:C0342388
a
ncit:C7057
.
dgn-gda:DGNbd07bb4da6c6702b5dd877ff4a437973
sio:SIO_000628
miriam-gene:5443
,
lld:C0342388
;
a
sio:SIO_001121
.
}
dgn-np:NP562192.RA_o9xK2pCpqrVPv4eYn9umMd_Nt2pELOhJQSXNWgQh84130_provenance
{
dgn-np:NP562192.RA_o9xK2pCpqrVPv4eYn9umMd_Nt2pELOhJQSXNWgQh84130_assertion
dcterms:description
"[This review will summarize recent findings that led to the first complete clinical description of inherited, isolated corticotropin (ACTH) deficiency (IAD) and to the first molecular mechanism for excessive ACTH production in Cushing's disease.]. 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:17718852
;
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:NP562192.RA_o9xK2pCpqrVPv4eYn9umMd_Nt2pELOhJQSXNWgQh84130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:39+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" .
}