@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP542219.RA6mUG_QuRgRBIbIrPkgASYsYNSwej2AOsWq5R0Wf_udE
> .
@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:NP542219.RA6mUG_QuRgRBIbIrPkgASYsYNSwej2AOsWq5R0Wf_udE130_head
{
this:
np:hasAssertion
dgn-np:NP542219.RA6mUG_QuRgRBIbIrPkgASYsYNSwej2AOsWq5R0Wf_udE130_assertion
;
np:hasProvenance
dgn-np:NP542219.RA6mUG_QuRgRBIbIrPkgASYsYNSwej2AOsWq5R0Wf_udE130_provenance
;
np:hasPublicationInfo
dgn-np:NP542219.RA6mUG_QuRgRBIbIrPkgASYsYNSwej2AOsWq5R0Wf_udE130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP542219.RA6mUG_QuRgRBIbIrPkgASYsYNSwej2AOsWq5R0Wf_udE130_assertion
a
np:Assertion
.
dgn-np:NP542219.RA6mUG_QuRgRBIbIrPkgASYsYNSwej2AOsWq5R0Wf_udE130_provenance
a
np:Provenance
.
dgn-np:NP542219.RA6mUG_QuRgRBIbIrPkgASYsYNSwej2AOsWq5R0Wf_udE130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP542219.RA6mUG_QuRgRBIbIrPkgASYsYNSwej2AOsWq5R0Wf_udE130_assertion
{
miriam-gene:57760
a
ncit:C16612
.
lld:C0034152
a
ncit:C7057
.
dgn-gda:DGN72ccd4bcc07cb2146972ce38b04bbb21
sio:SIO_000628
miriam-gene:57760
,
lld:C0034152
;
a
sio:SIO_001121
.
}
dgn-np:NP542219.RA6mUG_QuRgRBIbIrPkgASYsYNSwej2AOsWq5R0Wf_udE130_provenance
{
dgn-np:NP542219.RA6mUG_QuRgRBIbIrPkgASYsYNSwej2AOsWq5R0Wf_udE130_assertion
dcterms:description
"[More than 20 HSP loci and 10 spastic paraplegia genes (SPG) have been identified to date, including the genes responsible for the two most frequent forms of autosomal dominant spastic paraplegia (AD-HSP), encoding spastin (SPG4) and atlastin (SPG3A), respectively.]. 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:15517445
;
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:NP542219.RA6mUG_QuRgRBIbIrPkgASYsYNSwej2AOsWq5R0Wf_udE130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:27+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" .
}