@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP486252.RADoLXQ3p5Bxd9V_PhbvAl6r7fijO1vGktxf9E0ikNzmM
> .
@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:NP486252.RADoLXQ3p5Bxd9V_PhbvAl6r7fijO1vGktxf9E0ikNzmM130_head
{
this:
np:hasAssertion
dgn-np:NP486252.RADoLXQ3p5Bxd9V_PhbvAl6r7fijO1vGktxf9E0ikNzmM130_assertion
;
np:hasProvenance
dgn-np:NP486252.RADoLXQ3p5Bxd9V_PhbvAl6r7fijO1vGktxf9E0ikNzmM130_provenance
;
np:hasPublicationInfo
dgn-np:NP486252.RADoLXQ3p5Bxd9V_PhbvAl6r7fijO1vGktxf9E0ikNzmM130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP486252.RADoLXQ3p5Bxd9V_PhbvAl6r7fijO1vGktxf9E0ikNzmM130_assertion
a
np:Assertion
.
dgn-np:NP486252.RADoLXQ3p5Bxd9V_PhbvAl6r7fijO1vGktxf9E0ikNzmM130_provenance
a
np:Provenance
.
dgn-np:NP486252.RADoLXQ3p5Bxd9V_PhbvAl6r7fijO1vGktxf9E0ikNzmM130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP486252.RADoLXQ3p5Bxd9V_PhbvAl6r7fijO1vGktxf9E0ikNzmM130_assertion
{
miriam-gene:5376
a
ncit:C16612
.
lld:C0700251
a
ncit:C7057
.
dgn-gda:DGN041bcd05d71f72fa84bb3665f0749f25
sio:SIO_000628
miriam-gene:5376
,
lld:C0700251
;
a
sio:SIO_001121
.
}
dgn-np:NP486252.RADoLXQ3p5Bxd9V_PhbvAl6r7fijO1vGktxf9E0ikNzmM130_provenance
{
dgn-np:NP486252.RADoLXQ3p5Bxd9V_PhbvAl6r7fijO1vGktxf9E0ikNzmM130_assertion
dcterms:description
"[To determine whether hereditary neuropathy with liability to pressure palsies (HNPP) and inherited brachial plexus neuropathy (IBPN) are genetically distinct disorders and to evaluate the usefulness of fluorescence in situ hybridization (FISH) for diagnosing HNPP in individual 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:7630211
;
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:NP486252.RADoLXQ3p5Bxd9V_PhbvAl6r7fijO1vGktxf9E0ikNzmM130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:50+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" .
}