@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP752339.RAfDRmeAfoYGHAzABn3-fbrLSf1B0gZzGWXuK676_83mQ
> .
@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/v4.0.0/void/
> .
dgn-np:NP752339.RAfDRmeAfoYGHAzABn3-fbrLSf1B0gZzGWXuK676_83mQ130_head
{
this:
np:hasAssertion
dgn-np:NP752339.RAfDRmeAfoYGHAzABn3-fbrLSf1B0gZzGWXuK676_83mQ130_assertion
;
np:hasProvenance
dgn-np:NP752339.RAfDRmeAfoYGHAzABn3-fbrLSf1B0gZzGWXuK676_83mQ130_provenance
;
np:hasPublicationInfo
dgn-np:NP752339.RAfDRmeAfoYGHAzABn3-fbrLSf1B0gZzGWXuK676_83mQ130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP752339.RAfDRmeAfoYGHAzABn3-fbrLSf1B0gZzGWXuK676_83mQ130_assertion
a
np:Assertion
.
dgn-np:NP752339.RAfDRmeAfoYGHAzABn3-fbrLSf1B0gZzGWXuK676_83mQ130_provenance
a
np:Provenance
.
dgn-np:NP752339.RAfDRmeAfoYGHAzABn3-fbrLSf1B0gZzGWXuK676_83mQ130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP752339.RAfDRmeAfoYGHAzABn3-fbrLSf1B0gZzGWXuK676_83mQ130_assertion
{
miriam-gene:6683
a
ncit:C16612
.
lld:C0037773
a
ncit:C7057
.
dgn-gda:DGN95a97221eaf64103a48b5b42be27caf5
sio:SIO_000628
miriam-gene:6683
,
lld:C0037773
;
a
sio:SIO_001121
.
}
dgn-np:NP752339.RAfDRmeAfoYGHAzABn3-fbrLSf1B0gZzGWXuK676_83mQ130_provenance
{
dgn-np:NP752339.RAfDRmeAfoYGHAzABn3-fbrLSf1B0gZzGWXuK676_83mQ130_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-2016
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-2016
pav:importedOn
"2016-02-19"^^
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:NP752339.RAfDRmeAfoYGHAzABn3-fbrLSf1B0gZzGWXuK676_83mQ130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:47:26+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
"v4.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v4.0.0" .
}