@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP745459.RAXyTaVSd4zrzmweyC3sXSehxJHHBtvP3Ozw6LLqjdf4g
> .
@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:NP745459.RAXyTaVSd4zrzmweyC3sXSehxJHHBtvP3Ozw6LLqjdf4g130_head
{
this:
np:hasAssertion
dgn-np:NP745459.RAXyTaVSd4zrzmweyC3sXSehxJHHBtvP3Ozw6LLqjdf4g130_assertion
;
np:hasProvenance
dgn-np:NP745459.RAXyTaVSd4zrzmweyC3sXSehxJHHBtvP3Ozw6LLqjdf4g130_provenance
;
np:hasPublicationInfo
dgn-np:NP745459.RAXyTaVSd4zrzmweyC3sXSehxJHHBtvP3Ozw6LLqjdf4g130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP745459.RAXyTaVSd4zrzmweyC3sXSehxJHHBtvP3Ozw6LLqjdf4g130_assertion
a
np:Assertion
.
dgn-np:NP745459.RAXyTaVSd4zrzmweyC3sXSehxJHHBtvP3Ozw6LLqjdf4g130_provenance
a
np:Provenance
.
dgn-np:NP745459.RAXyTaVSd4zrzmweyC3sXSehxJHHBtvP3Ozw6LLqjdf4g130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP745459.RAXyTaVSd4zrzmweyC3sXSehxJHHBtvP3Ozw6LLqjdf4g130_assertion
{
miriam-gene:3798
a
ncit:C16612
.
lld:C0037773
a
ncit:C7057
.
dgn-gda:DGN0678b42a889ba6b4944fe43ffadd999e
sio:SIO_000628
miriam-gene:3798
,
lld:C0037773
;
a
sio:SIO_001121
.
}
dgn-np:NP745459.RAXyTaVSd4zrzmweyC3sXSehxJHHBtvP3Ozw6LLqjdf4g130_provenance
{
dgn-np:NP745459.RAXyTaVSd4zrzmweyC3sXSehxJHHBtvP3Ozw6LLqjdf4g130_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:NP745459.RAXyTaVSd4zrzmweyC3sXSehxJHHBtvP3Ozw6LLqjdf4g130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:32+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" .
}