@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP933052.RA7h1MmZDPRn9wyDm9ou-bd-Fli2EC7gBBYzk3sGEbb2A
> .
@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:NP933052.RA7h1MmZDPRn9wyDm9ou-bd-Fli2EC7gBBYzk3sGEbb2A130_head
{
this:
np:hasAssertion
dgn-np:NP933052.RA7h1MmZDPRn9wyDm9ou-bd-Fli2EC7gBBYzk3sGEbb2A130_assertion
;
np:hasProvenance
dgn-np:NP933052.RA7h1MmZDPRn9wyDm9ou-bd-Fli2EC7gBBYzk3sGEbb2A130_provenance
;
np:hasPublicationInfo
dgn-np:NP933052.RA7h1MmZDPRn9wyDm9ou-bd-Fli2EC7gBBYzk3sGEbb2A130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP933052.RA7h1MmZDPRn9wyDm9ou-bd-Fli2EC7gBBYzk3sGEbb2A130_assertion
a
np:Assertion
.
dgn-np:NP933052.RA7h1MmZDPRn9wyDm9ou-bd-Fli2EC7gBBYzk3sGEbb2A130_provenance
a
np:Provenance
.
dgn-np:NP933052.RA7h1MmZDPRn9wyDm9ou-bd-Fli2EC7gBBYzk3sGEbb2A130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP933052.RA7h1MmZDPRn9wyDm9ou-bd-Fli2EC7gBBYzk3sGEbb2A130_assertion
{
miriam-gene:3918
a
ncit:C16612
.
lld:C0442874
a
ncit:C7057
.
dgn-gda:DGNa701fc23505f01802a6e57a8602167b8
sio:SIO_000628
miriam-gene:3918
,
lld:C0442874
;
a
sio:SIO_001121
.
}
dgn-np:NP933052.RA7h1MmZDPRn9wyDm9ou-bd-Fli2EC7gBBYzk3sGEbb2A130_provenance
{
dgn-np:NP933052.RA7h1MmZDPRn9wyDm9ou-bd-Fli2EC7gBBYzk3sGEbb2A130_assertion
dcterms:description
"[In a retrospective study, we identified 15 consecutive HIV-positive patients with a diagnosis of CMV-MN based on (1) markedly asymmetric neuropathy, (2) fewer than 100 CD4+ cells per mm3, (3) exclusion of other causes of neuropathy, and (4) characteristic CMV cytopathic changes on neuromuscular biopsy (2 patients), positive CSF culture for CMV (2 patients), or clinical improvement on anti-CMV therapy given for concurrent extraneurologic CMV disease (8 patients) or neuropathy (3 patients).]. 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:7969979
;
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:NP933052.RA7h1MmZDPRn9wyDm9ou-bd-Fli2EC7gBBYzk3sGEbb2A130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:41:32+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" .
}