@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP359913.RANbDS_F-KS92W0ktRQJIGublOGUuDFnuk_6I9bXfzzbY
> .
@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:NP359913.RANbDS_F-KS92W0ktRQJIGublOGUuDFnuk_6I9bXfzzbY130_head
{
this:
np:hasAssertion
dgn-np:NP359913.RANbDS_F-KS92W0ktRQJIGublOGUuDFnuk_6I9bXfzzbY130_assertion
;
np:hasProvenance
dgn-np:NP359913.RANbDS_F-KS92W0ktRQJIGublOGUuDFnuk_6I9bXfzzbY130_provenance
;
np:hasPublicationInfo
dgn-np:NP359913.RANbDS_F-KS92W0ktRQJIGublOGUuDFnuk_6I9bXfzzbY130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP359913.RANbDS_F-KS92W0ktRQJIGublOGUuDFnuk_6I9bXfzzbY130_assertion
a
np:Assertion
.
dgn-np:NP359913.RANbDS_F-KS92W0ktRQJIGublOGUuDFnuk_6I9bXfzzbY130_provenance
a
np:Provenance
.
dgn-np:NP359913.RANbDS_F-KS92W0ktRQJIGublOGUuDFnuk_6I9bXfzzbY130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP359913.RANbDS_F-KS92W0ktRQJIGublOGUuDFnuk_6I9bXfzzbY130_assertion
{
miriam-gene:4397
a
ncit:C16612
.
lld:C0740279
a
ncit:C7057
.
dgn-gda:DGN4b045e6c8dd1d911199a19f679017990
sio:SIO_000628
miriam-gene:4397
,
lld:C0740279
;
a
sio:SIO_001121
.
}
dgn-np:NP359913.RANbDS_F-KS92W0ktRQJIGublOGUuDFnuk_6I9bXfzzbY130_provenance
{
dgn-np:NP359913.RANbDS_F-KS92W0ktRQJIGublOGUuDFnuk_6I9bXfzzbY130_assertion
dcterms:description
"[The multiple sclerosis group with severe cerebellar deficit and the ADCA group both had significant cerebellar atrophy (suggesting nerve cell body and axon loss) compared with the multiple sclerosis patients with minimal or no signs of cerebellar deficit and healthy controls.]. 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:8595487
;
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:NP359913.RANbDS_F-KS92W0ktRQJIGublOGUuDFnuk_6I9bXfzzbY130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:31+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" .
}