@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP269822.RAzfxH8VfRw4AfTTBvCc2NPexFuu5BWlj8UVpDYC01RiQ
> .
@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:NP269822.RAzfxH8VfRw4AfTTBvCc2NPexFuu5BWlj8UVpDYC01RiQ130_head
{
this:
np:hasAssertion
dgn-np:NP269822.RAzfxH8VfRw4AfTTBvCc2NPexFuu5BWlj8UVpDYC01RiQ130_assertion
;
np:hasProvenance
dgn-np:NP269822.RAzfxH8VfRw4AfTTBvCc2NPexFuu5BWlj8UVpDYC01RiQ130_provenance
;
np:hasPublicationInfo
dgn-np:NP269822.RAzfxH8VfRw4AfTTBvCc2NPexFuu5BWlj8UVpDYC01RiQ130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP269822.RAzfxH8VfRw4AfTTBvCc2NPexFuu5BWlj8UVpDYC01RiQ130_assertion
a
np:Assertion
.
dgn-np:NP269822.RAzfxH8VfRw4AfTTBvCc2NPexFuu5BWlj8UVpDYC01RiQ130_provenance
a
np:Provenance
.
dgn-np:NP269822.RAzfxH8VfRw4AfTTBvCc2NPexFuu5BWlj8UVpDYC01RiQ130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP269822.RAzfxH8VfRw4AfTTBvCc2NPexFuu5BWlj8UVpDYC01RiQ130_assertion
{
miriam-gene:5443
a
ncit:C16612
.
lld:C0027577
a
ncit:C7057
.
dgn-gda:DGNf3f57df5a06b022f573733bf42b7bd1d
sio:SIO_000628
miriam-gene:5443
,
lld:C0027577
;
a
sio:SIO_001121
.
}
dgn-np:NP269822.RAzfxH8VfRw4AfTTBvCc2NPexFuu5BWlj8UVpDYC01RiQ130_provenance
{
dgn-np:NP269822.RAzfxH8VfRw4AfTTBvCc2NPexFuu5BWlj8UVpDYC01RiQ130_assertion
dcterms:description
"[We have analyzed the upstream promoter region of POMC gene from eleven patients with Cushing's disease, four of which had Nelson's syndrome, and from one patient with an ectopic ACTH syndrome secondary to a lung carcinoid for any possible mutations in the nGRE and/or cAMP-responsive sequences.]. 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:8386673
;
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:NP269822.RAzfxH8VfRw4AfTTBvCc2NPexFuu5BWlj8UVpDYC01RiQ130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:30+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" .
}