@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP728394.RA0D2NLXKAqtaR4pA7dA5IB5p7ceD9npqk7eNhvN9gDQg
> .
@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:NP728394.RA0D2NLXKAqtaR4pA7dA5IB5p7ceD9npqk7eNhvN9gDQg130_head
{
this:
np:hasAssertion
dgn-np:NP728394.RA0D2NLXKAqtaR4pA7dA5IB5p7ceD9npqk7eNhvN9gDQg130_assertion
;
np:hasProvenance
dgn-np:NP728394.RA0D2NLXKAqtaR4pA7dA5IB5p7ceD9npqk7eNhvN9gDQg130_provenance
;
np:hasPublicationInfo
dgn-np:NP728394.RA0D2NLXKAqtaR4pA7dA5IB5p7ceD9npqk7eNhvN9gDQg130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP728394.RA0D2NLXKAqtaR4pA7dA5IB5p7ceD9npqk7eNhvN9gDQg130_assertion
a
np:Assertion
.
dgn-np:NP728394.RA0D2NLXKAqtaR4pA7dA5IB5p7ceD9npqk7eNhvN9gDQg130_provenance
a
np:Provenance
.
dgn-np:NP728394.RA0D2NLXKAqtaR4pA7dA5IB5p7ceD9npqk7eNhvN9gDQg130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP728394.RA0D2NLXKAqtaR4pA7dA5IB5p7ceD9npqk7eNhvN9gDQg130_assertion
{
miriam-gene:3799
a
ncit:C16612
.
lld:C0037773
a
ncit:C7057
.
dgn-gda:DGN30491afbdb1441964ec256f3e62cc4b1
sio:SIO_000628
miriam-gene:3799
,
lld:C0037773
;
a
sio:SIO_001121
.
}
dgn-np:NP728394.RA0D2NLXKAqtaR4pA7dA5IB5p7ceD9npqk7eNhvN9gDQg130_provenance
{
dgn-np:NP728394.RA0D2NLXKAqtaR4pA7dA5IB5p7ceD9npqk7eNhvN9gDQg130_assertion
dcterms:description
"[SPG10 is an autosomal dominant form of hereditary spastic paraplegia (HSP), which is caused by mutations in the neural kinesin heavy chain KIF5A gene, the neuronal motor of fast anterograde axonal transport.]. 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:18245137
;
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:NP728394.RA0D2NLXKAqtaR4pA7dA5IB5p7ceD9npqk7eNhvN9gDQg130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:22+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" .
}