@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP1373794.RAgJ9f1Jc8wX62fawkOqMYVIyyycb6XJ9kR0d-7JjwucQ
> .
@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/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@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/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v4.0.0/void/
> .
dgn-np:NP1373794.RAgJ9f1Jc8wX62fawkOqMYVIyyycb6XJ9kR0d-7JjwucQ130_head
{
this:
np:hasAssertion
dgn-np:NP1373794.RAgJ9f1Jc8wX62fawkOqMYVIyyycb6XJ9kR0d-7JjwucQ130_assertion
;
np:hasProvenance
dgn-np:NP1373794.RAgJ9f1Jc8wX62fawkOqMYVIyyycb6XJ9kR0d-7JjwucQ130_provenance
;
np:hasPublicationInfo
dgn-np:NP1373794.RAgJ9f1Jc8wX62fawkOqMYVIyyycb6XJ9kR0d-7JjwucQ130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP1373794.RAgJ9f1Jc8wX62fawkOqMYVIyyycb6XJ9kR0d-7JjwucQ130_assertion
a
np:Assertion
.
dgn-np:NP1373794.RAgJ9f1Jc8wX62fawkOqMYVIyyycb6XJ9kR0d-7JjwucQ130_provenance
a
np:Provenance
.
dgn-np:NP1373794.RAgJ9f1Jc8wX62fawkOqMYVIyyycb6XJ9kR0d-7JjwucQ130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP1373794.RAgJ9f1Jc8wX62fawkOqMYVIyyycb6XJ9kR0d-7JjwucQ130_assertion
{
miriam-gene:4158
a
ncit:C16612
.
lld:C0271742
a
ncit:C7057
.
dgn-gda:DGNed477ed85ad5b5dd2b6f1982f04e49cd
sio:SIO_000628
miriam-gene:4158
,
lld:C0271742
;
a
sio:SIO_001121
.
}
dgn-np:NP1373794.RAgJ9f1Jc8wX62fawkOqMYVIyyycb6XJ9kR0d-7JjwucQ130_provenance
{
dgn-np:NP1373794.RAgJ9f1Jc8wX62fawkOqMYVIyyycb6XJ9kR0d-7JjwucQ130_assertion
dcterms:description
"[Interestingly, ACTH receptor mutations are not present in all patients with FGD and also not in the closely related triple A' syndrome indicating that other mechanisms of ACTH resistance are still to be elucidated.]. 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:9167964
;
prov:wasDerivedFrom
dgn-void:befree-2016
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-2016
pav:importedOn
"2016-02-19"^^
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:NP1373794.RAgJ9f1Jc8wX62fawkOqMYVIyyycb6XJ9kR0d-7JjwucQ130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:52:08+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:disgenetv3.0rdf
;
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
"v4.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v4.0.0" .
}