@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP499572.RA8F6X04Ds6noKnJZ4yBj4JwnrPnYTDmoQCqkgoUPHrBU
> .
@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:NP499572.RA8F6X04Ds6noKnJZ4yBj4JwnrPnYTDmoQCqkgoUPHrBU130_head
{
this:
np:hasAssertion
dgn-np:NP499572.RA8F6X04Ds6noKnJZ4yBj4JwnrPnYTDmoQCqkgoUPHrBU130_assertion
;
np:hasProvenance
dgn-np:NP499572.RA8F6X04Ds6noKnJZ4yBj4JwnrPnYTDmoQCqkgoUPHrBU130_provenance
;
np:hasPublicationInfo
dgn-np:NP499572.RA8F6X04Ds6noKnJZ4yBj4JwnrPnYTDmoQCqkgoUPHrBU130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP499572.RA8F6X04Ds6noKnJZ4yBj4JwnrPnYTDmoQCqkgoUPHrBU130_assertion
a
np:Assertion
.
dgn-np:NP499572.RA8F6X04Ds6noKnJZ4yBj4JwnrPnYTDmoQCqkgoUPHrBU130_provenance
a
np:Provenance
.
dgn-np:NP499572.RA8F6X04Ds6noKnJZ4yBj4JwnrPnYTDmoQCqkgoUPHrBU130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP499572.RA8F6X04Ds6noKnJZ4yBj4JwnrPnYTDmoQCqkgoUPHrBU130_assertion
{
miriam-gene:4359
a
ncit:C16612
.
lld:C0031117
a
ncit:C7057
.
dgn-gda:DGNa950311955e044335b60ca5b991ccb8c
sio:SIO_000628
miriam-gene:4359
,
lld:C0031117
;
a
sio:SIO_001121
.
}
dgn-np:NP499572.RA8F6X04Ds6noKnJZ4yBj4JwnrPnYTDmoQCqkgoUPHrBU130_provenance
{
dgn-np:NP499572.RA8F6X04Ds6noKnJZ4yBj4JwnrPnYTDmoQCqkgoUPHrBU130_assertion
dcterms:description
"[The understanding of the molecular basis of CMT1 and related disorders has allowed accurate DNA diagnosis and genetic counseling of inherited peripheral neuropathies and will make it possible to develop rational strategies for therapy.]. 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:8862346
;
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:NP499572.RA8F6X04Ds6noKnJZ4yBj4JwnrPnYTDmoQCqkgoUPHrBU130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:58+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" .
}