@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP769220.RAtUTgzJ2iYYMTQ6AR2gYd8cu-Q_rtRueHXHteCGkwPoE
> .
@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:NP769220.RAtUTgzJ2iYYMTQ6AR2gYd8cu-Q_rtRueHXHteCGkwPoE130_head
{
this:
np:hasAssertion
dgn-np:NP769220.RAtUTgzJ2iYYMTQ6AR2gYd8cu-Q_rtRueHXHteCGkwPoE130_assertion
;
np:hasProvenance
dgn-np:NP769220.RAtUTgzJ2iYYMTQ6AR2gYd8cu-Q_rtRueHXHteCGkwPoE130_provenance
;
np:hasPublicationInfo
dgn-np:NP769220.RAtUTgzJ2iYYMTQ6AR2gYd8cu-Q_rtRueHXHteCGkwPoE130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP769220.RAtUTgzJ2iYYMTQ6AR2gYd8cu-Q_rtRueHXHteCGkwPoE130_assertion
a
np:Assertion
.
dgn-np:NP769220.RAtUTgzJ2iYYMTQ6AR2gYd8cu-Q_rtRueHXHteCGkwPoE130_provenance
a
np:Provenance
.
dgn-np:NP769220.RAtUTgzJ2iYYMTQ6AR2gYd8cu-Q_rtRueHXHteCGkwPoE130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP769220.RAtUTgzJ2iYYMTQ6AR2gYd8cu-Q_rtRueHXHteCGkwPoE130_assertion
{
miriam-gene:6683
a
ncit:C16612
.
lld:C0338656
a
ncit:C7057
.
dgn-gda:DGN431a587ef4c8d2d08575a55e8d3fd2cd
sio:SIO_000628
miriam-gene:6683
,
lld:C0338656
;
a
sio:SIO_001121
.
}
dgn-np:NP769220.RAtUTgzJ2iYYMTQ6AR2gYd8cu-Q_rtRueHXHteCGkwPoE130_provenance
{
dgn-np:NP769220.RAtUTgzJ2iYYMTQ6AR2gYd8cu-Q_rtRueHXHteCGkwPoE130_assertion
dcterms:description
"[The demonstration of widespread distribution of spastin in functionally different brain regions in the present study may provide neuroanatomical basis to explain why different neurological, psychological disorders and cognitive impairment occur in patients with spastin mutation.]. 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:16828199
;
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:NP769220.RAtUTgzJ2iYYMTQ6AR2gYd8cu-Q_rtRueHXHteCGkwPoE130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:45+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" .
}