@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP842568.RAoyiffOor8Z5cUnCqFw2msPEP90LDVtRqPsmlR93sLYQ
> .
@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/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@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/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v3.0.0/void/
> .
dgn-np:NP842568.RAoyiffOor8Z5cUnCqFw2msPEP90LDVtRqPsmlR93sLYQ130_head
{
this:
np:hasAssertion
dgn-np:NP842568.RAoyiffOor8Z5cUnCqFw2msPEP90LDVtRqPsmlR93sLYQ130_assertion
;
np:hasProvenance
dgn-np:NP842568.RAoyiffOor8Z5cUnCqFw2msPEP90LDVtRqPsmlR93sLYQ130_provenance
;
np:hasPublicationInfo
dgn-np:NP842568.RAoyiffOor8Z5cUnCqFw2msPEP90LDVtRqPsmlR93sLYQ130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP842568.RAoyiffOor8Z5cUnCqFw2msPEP90LDVtRqPsmlR93sLYQ130_assertion
a
np:Assertion
.
dgn-np:NP842568.RAoyiffOor8Z5cUnCqFw2msPEP90LDVtRqPsmlR93sLYQ130_provenance
a
np:Provenance
.
dgn-np:NP842568.RAoyiffOor8Z5cUnCqFw2msPEP90LDVtRqPsmlR93sLYQ130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP842568.RAoyiffOor8Z5cUnCqFw2msPEP90LDVtRqPsmlR93sLYQ130_assertion
{
miriam-gene:10397
a
ncit:C16612
.
lld:C0007959
a
ncit:C7057
.
dgn-gda:DGNa0eb96d069eae9bd0caba273d625170b
sio:SIO_000628
miriam-gene:10397
,
lld:C0007959
;
a
sio:SIO_001121
.
}
dgn-np:NP842568.RAoyiffOor8Z5cUnCqFw2msPEP90LDVtRqPsmlR93sLYQ130_provenance
{
dgn-np:NP842568.RAoyiffOor8Z5cUnCqFw2msPEP90LDVtRqPsmlR93sLYQ130_assertion
dcterms:description
"[The success of molecular genetic analysis in all families confirms that autosomal recessive forms of CMT caused by mutations on the NDRG1 and HK1 genes are common causes of inherited neuropathies among Slovak Roma.]. 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:23996628
;
prov:wasDerivedFrom
dgn-void:befree-20150227
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-20150227
pav:importedOn
"2015-02-27"^^
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:NP842568.RAoyiffOor8Z5cUnCqFw2msPEP90LDVtRqPsmlR93sLYQ130_publicationInfo
{
this:
dcterms:created
"2015-08-25T14:46:11+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:disgenetv3.0rdf
;
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
"v3.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v3.0.0" .
}