@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP307984.RAClQATguM5EQXxwcTw3Xcubdgp09qfpkboKtttxnJlJY
> .
@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:NP307984.RAClQATguM5EQXxwcTw3Xcubdgp09qfpkboKtttxnJlJY130_head
{
this:
np:hasAssertion
dgn-np:NP307984.RAClQATguM5EQXxwcTw3Xcubdgp09qfpkboKtttxnJlJY130_assertion
;
np:hasProvenance
dgn-np:NP307984.RAClQATguM5EQXxwcTw3Xcubdgp09qfpkboKtttxnJlJY130_provenance
;
np:hasPublicationInfo
dgn-np:NP307984.RAClQATguM5EQXxwcTw3Xcubdgp09qfpkboKtttxnJlJY130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP307984.RAClQATguM5EQXxwcTw3Xcubdgp09qfpkboKtttxnJlJY130_assertion
a
np:Assertion
.
dgn-np:NP307984.RAClQATguM5EQXxwcTw3Xcubdgp09qfpkboKtttxnJlJY130_provenance
a
np:Provenance
.
dgn-np:NP307984.RAClQATguM5EQXxwcTw3Xcubdgp09qfpkboKtttxnJlJY130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP307984.RAClQATguM5EQXxwcTw3Xcubdgp09qfpkboKtttxnJlJY130_assertion
{
miriam-gene:4359
a
ncit:C16612
.
lld:C0270912
a
ncit:C7057
.
dgn-gda:DGN2d79f4bb1af38794f240b50f704fdb58
sio:SIO_000628
miriam-gene:4359
,
lld:C0270912
;
a
sio:SIO_001121
.
}
dgn-np:NP307984.RAClQATguM5EQXxwcTw3Xcubdgp09qfpkboKtttxnJlJY130_provenance
{
dgn-np:NP307984.RAClQATguM5EQXxwcTw3Xcubdgp09qfpkboKtttxnJlJY130_assertion
dcterms:description
"[Identifying molecular pathways involved in early and late onset CMT1B will be crucial to understand how MPZ mutations cause CMT1B so that rational therapies for both early and late onset neuropathies can be developed.]. 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:16414078
;
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:NP307984.RAClQATguM5EQXxwcTw3Xcubdgp09qfpkboKtttxnJlJY130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:56+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" .
}