@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP710077.RAibCqir-eD6hzKS7TPSUgKOvK1mE39NEb5otiTtt3GQk
> .
@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/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@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/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v3.0.0/void/
> .
dgn-np:NP710077.RAibCqir-eD6hzKS7TPSUgKOvK1mE39NEb5otiTtt3GQk130_head
{
this:
np:hasAssertion
dgn-np:NP710077.RAibCqir-eD6hzKS7TPSUgKOvK1mE39NEb5otiTtt3GQk130_assertion
;
np:hasProvenance
dgn-np:NP710077.RAibCqir-eD6hzKS7TPSUgKOvK1mE39NEb5otiTtt3GQk130_provenance
;
np:hasPublicationInfo
dgn-np:NP710077.RAibCqir-eD6hzKS7TPSUgKOvK1mE39NEb5otiTtt3GQk130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP710077.RAibCqir-eD6hzKS7TPSUgKOvK1mE39NEb5otiTtt3GQk130_assertion
a
np:Assertion
.
dgn-np:NP710077.RAibCqir-eD6hzKS7TPSUgKOvK1mE39NEb5otiTtt3GQk130_provenance
a
np:Provenance
.
dgn-np:NP710077.RAibCqir-eD6hzKS7TPSUgKOvK1mE39NEb5otiTtt3GQk130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP710077.RAibCqir-eD6hzKS7TPSUgKOvK1mE39NEb5otiTtt3GQk130_assertion
{
miriam-gene:6683
a
ncit:C16612
.
lld:C3714552
a
ncit:C7057
.
dgn-gda:DGN908c1521711a8ae02bf9f6e112a4c446
sio:SIO_000628
miriam-gene:6683
,
lld:C3714552
;
a
sio:SIO_001121
.
}
dgn-np:NP710077.RAibCqir-eD6hzKS7TPSUgKOvK1mE39NEb5otiTtt3GQk130_provenance
{
dgn-np:NP710077.RAibCqir-eD6hzKS7TPSUgKOvK1mE39NEb5otiTtt3GQk130_assertion
dcterms:description
"[Mutations of human spastin, an AAA (ATPases associated with diverse cellular activity) family protein, cause an autosomal dominant form of hereditary spastic paraplegia, which is characterized by weakness, spasticity and loss of the vibratory sense in the lower limbs.]. 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:19619244
;
prov:wasDerivedFrom
dgn-void:befree-20150227
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-20150227
pav:importedOn
"2015-02-27"^^
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:NP710077.RAibCqir-eD6hzKS7TPSUgKOvK1mE39NEb5otiTtt3GQk130_publicationInfo
{
this:
dcterms:created
"2015-08-25T14:44:48+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:disgenetv3.0rdf
;
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
"v3.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v3.0.0" .
}