@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP667461.RAvVjE9Uqt4OhDmZGsU3EcnqcQpDLDgYh8ZI1dn6xqlZM
> .
@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:NP667461.RAvVjE9Uqt4OhDmZGsU3EcnqcQpDLDgYh8ZI1dn6xqlZM130_head
{
this:
np:hasAssertion
dgn-np:NP667461.RAvVjE9Uqt4OhDmZGsU3EcnqcQpDLDgYh8ZI1dn6xqlZM130_assertion
;
np:hasProvenance
dgn-np:NP667461.RAvVjE9Uqt4OhDmZGsU3EcnqcQpDLDgYh8ZI1dn6xqlZM130_provenance
;
np:hasPublicationInfo
dgn-np:NP667461.RAvVjE9Uqt4OhDmZGsU3EcnqcQpDLDgYh8ZI1dn6xqlZM130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP667461.RAvVjE9Uqt4OhDmZGsU3EcnqcQpDLDgYh8ZI1dn6xqlZM130_assertion
a
np:Assertion
.
dgn-np:NP667461.RAvVjE9Uqt4OhDmZGsU3EcnqcQpDLDgYh8ZI1dn6xqlZM130_provenance
a
np:Provenance
.
dgn-np:NP667461.RAvVjE9Uqt4OhDmZGsU3EcnqcQpDLDgYh8ZI1dn6xqlZM130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP667461.RAvVjE9Uqt4OhDmZGsU3EcnqcQpDLDgYh8ZI1dn6xqlZM130_assertion
{
miriam-gene:2705
a
ncit:C16612
.
lld:C0270922
a
ncit:C7057
.
dgn-gda:DGN6ad0dbba4c49c32ef63ad0a5cee35c55
sio:SIO_000628
miriam-gene:2705
,
lld:C0270922
;
a
sio:SIO_001121
.
}
dgn-np:NP667461.RAvVjE9Uqt4OhDmZGsU3EcnqcQpDLDgYh8ZI1dn6xqlZM130_provenance
{
dgn-np:NP667461.RAvVjE9Uqt4OhDmZGsU3EcnqcQpDLDgYh8ZI1dn6xqlZM130_assertion
dcterms:description
"[In the past few years a number of inherited demyelinating neuropathies in mice and the human have been shown to be due to mutations affecting the genes PMP22, Po and Cx32 so that it has become possible to characterise the molecular pathology of the majority of these disorders.]. 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:7559122
;
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:NP667461.RAvVjE9Uqt4OhDmZGsU3EcnqcQpDLDgYh8ZI1dn6xqlZM130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:43+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" .
}