@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP266207.RAfkNX9UnwLxjFcmtUa_1rhvkmgbJEs39-mUVu1fWoFkk
> .
@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:NP266207.RAfkNX9UnwLxjFcmtUa_1rhvkmgbJEs39-mUVu1fWoFkk130_head
{
this:
np:hasAssertion
dgn-np:NP266207.RAfkNX9UnwLxjFcmtUa_1rhvkmgbJEs39-mUVu1fWoFkk130_assertion
;
np:hasProvenance
dgn-np:NP266207.RAfkNX9UnwLxjFcmtUa_1rhvkmgbJEs39-mUVu1fWoFkk130_provenance
;
np:hasPublicationInfo
dgn-np:NP266207.RAfkNX9UnwLxjFcmtUa_1rhvkmgbJEs39-mUVu1fWoFkk130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP266207.RAfkNX9UnwLxjFcmtUa_1rhvkmgbJEs39-mUVu1fWoFkk130_assertion
a
np:Assertion
.
dgn-np:NP266207.RAfkNX9UnwLxjFcmtUa_1rhvkmgbJEs39-mUVu1fWoFkk130_provenance
a
np:Provenance
.
dgn-np:NP266207.RAfkNX9UnwLxjFcmtUa_1rhvkmgbJEs39-mUVu1fWoFkk130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP266207.RAfkNX9UnwLxjFcmtUa_1rhvkmgbJEs39-mUVu1fWoFkk130_assertion
{
miriam-gene:6683
a
ncit:C16612
.
lld:C0443306
a
ncit:C7057
.
dgn-gda:DGNfe2c4e88b401efe33db5004ebbe1bf06
sio:SIO_000628
miriam-gene:6683
,
lld:C0443306
;
a
sio:SIO_001121
.
}
dgn-np:NP266207.RAfkNX9UnwLxjFcmtUa_1rhvkmgbJEs39-mUVu1fWoFkk130_provenance
{
dgn-np:NP266207.RAfkNX9UnwLxjFcmtUa_1rhvkmgbJEs39-mUVu1fWoFkk130_assertion
dcterms:description
"[The most common forms of hereditary spastic paraplaegia are SPG4 and SPG3A caused by sequence variants in the SPAST and ATL1 genes, as well as by deletions and duplications not detected by standard techniques.]. 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:22203332
;
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:NP266207.RAfkNX9UnwLxjFcmtUa_1rhvkmgbJEs39-mUVu1fWoFkk130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:28+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" .
}