@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP311291.RAX7fI6EXCwdrOLuMGnWa0qQ0Wcb1QLk78qRpvR8MBW4Y
> .
@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:NP311291.RAX7fI6EXCwdrOLuMGnWa0qQ0Wcb1QLk78qRpvR8MBW4Y130_head
{
this:
np:hasAssertion
dgn-np:NP311291.RAX7fI6EXCwdrOLuMGnWa0qQ0Wcb1QLk78qRpvR8MBW4Y130_assertion
;
np:hasProvenance
dgn-np:NP311291.RAX7fI6EXCwdrOLuMGnWa0qQ0Wcb1QLk78qRpvR8MBW4Y130_provenance
;
np:hasPublicationInfo
dgn-np:NP311291.RAX7fI6EXCwdrOLuMGnWa0qQ0Wcb1QLk78qRpvR8MBW4Y130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP311291.RAX7fI6EXCwdrOLuMGnWa0qQ0Wcb1QLk78qRpvR8MBW4Y130_assertion
a
np:Assertion
.
dgn-np:NP311291.RAX7fI6EXCwdrOLuMGnWa0qQ0Wcb1QLk78qRpvR8MBW4Y130_provenance
a
np:Provenance
.
dgn-np:NP311291.RAX7fI6EXCwdrOLuMGnWa0qQ0Wcb1QLk78qRpvR8MBW4Y130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP311291.RAX7fI6EXCwdrOLuMGnWa0qQ0Wcb1QLk78qRpvR8MBW4Y130_assertion
{
miriam-gene:4397
a
ncit:C16612
.
lld:C0023520
a
ncit:C7057
.
dgn-gda:DGN66bb220c7165d788b7cdf37d80681efe
sio:SIO_000628
miriam-gene:4397
,
lld:C0023520
;
a
sio:SIO_001121
.
}
dgn-np:NP311291.RAX7fI6EXCwdrOLuMGnWa0qQ0Wcb1QLk78qRpvR8MBW4Y130_provenance
{
dgn-np:NP311291.RAX7fI6EXCwdrOLuMGnWa0qQ0Wcb1QLk78qRpvR8MBW4Y130_assertion
dcterms:description
"[Demyelination caused by injury or disease together with failure of myelin regeneration disrupts the rapid propagation of action potentials along nerve fibers, and is associated with acquired and inherited disorders, including devastating multiple sclerosis and leukodystrophies.]. 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:23494530
;
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:NP311291.RAX7fI6EXCwdrOLuMGnWa0qQ0Wcb1QLk78qRpvR8MBW4Y130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:58+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" .
}