@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP369507.RA3iQG4-0yIUgzXp81duMDL_yRXpKjNvf53q7dugEeO5k
> .
@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:NP369507.RA3iQG4-0yIUgzXp81duMDL_yRXpKjNvf53q7dugEeO5k130_head
{
this:
np:hasAssertion
dgn-np:NP369507.RA3iQG4-0yIUgzXp81duMDL_yRXpKjNvf53q7dugEeO5k130_assertion
;
np:hasProvenance
dgn-np:NP369507.RA3iQG4-0yIUgzXp81duMDL_yRXpKjNvf53q7dugEeO5k130_provenance
;
np:hasPublicationInfo
dgn-np:NP369507.RA3iQG4-0yIUgzXp81duMDL_yRXpKjNvf53q7dugEeO5k130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP369507.RA3iQG4-0yIUgzXp81duMDL_yRXpKjNvf53q7dugEeO5k130_assertion
a
np:Assertion
.
dgn-np:NP369507.RA3iQG4-0yIUgzXp81duMDL_yRXpKjNvf53q7dugEeO5k130_provenance
a
np:Provenance
.
dgn-np:NP369507.RA3iQG4-0yIUgzXp81duMDL_yRXpKjNvf53q7dugEeO5k130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP369507.RA3iQG4-0yIUgzXp81duMDL_yRXpKjNvf53q7dugEeO5k130_assertion
{
miriam-gene:5443
a
ncit:C16612
.
lld:C1527231
a
ncit:C7057
.
dgn-gda:DGNa20d23a467703d86829dbb0fd17817ea
sio:SIO_000628
miriam-gene:5443
,
lld:C1527231
;
a
sio:SIO_001121
.
}
dgn-np:NP369507.RA3iQG4-0yIUgzXp81duMDL_yRXpKjNvf53q7dugEeO5k130_provenance
{
dgn-np:NP369507.RA3iQG4-0yIUgzXp81duMDL_yRXpKjNvf53q7dugEeO5k130_assertion
dcterms:description
"[Although on examination by light microscopy the sural nerve proved to be normal, the clinical diagnosis of adrenomyeloneuropathy (AMN) in its juvenile form may be assumed, in view of the clinical symptoms and the evidence of adrenocortical insufficiency revealed by the ACTH test.]. 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:6164756
;
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:NP369507.RA3iQG4-0yIUgzXp81duMDL_yRXpKjNvf53q7dugEeO5k130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:36+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" .
}