@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP383248.RAnvchppR97z1o44HPTg_rpEMyuS0s7uyZRF8OIE830AI
> .
@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:NP383248.RAnvchppR97z1o44HPTg_rpEMyuS0s7uyZRF8OIE830AI130_head
{
this:
np:hasAssertion
dgn-np:NP383248.RAnvchppR97z1o44HPTg_rpEMyuS0s7uyZRF8OIE830AI130_assertion
;
np:hasProvenance
dgn-np:NP383248.RAnvchppR97z1o44HPTg_rpEMyuS0s7uyZRF8OIE830AI130_provenance
;
np:hasPublicationInfo
dgn-np:NP383248.RAnvchppR97z1o44HPTg_rpEMyuS0s7uyZRF8OIE830AI130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP383248.RAnvchppR97z1o44HPTg_rpEMyuS0s7uyZRF8OIE830AI130_assertion
a
np:Assertion
.
dgn-np:NP383248.RAnvchppR97z1o44HPTg_rpEMyuS0s7uyZRF8OIE830AI130_provenance
a
np:Provenance
.
dgn-np:NP383248.RAnvchppR97z1o44HPTg_rpEMyuS0s7uyZRF8OIE830AI130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP383248.RAnvchppR97z1o44HPTg_rpEMyuS0s7uyZRF8OIE830AI130_assertion
{
miriam-gene:6683
a
ncit:C16612
.
lld:C0037772
a
ncit:C7057
.
dgn-gda:DGNf1bebf9c59c24c9ebdd6e6f0e3207ed3
sio:SIO_000628
miriam-gene:6683
,
lld:C0037772
;
a
sio:SIO_001121
.
}
dgn-np:NP383248.RAnvchppR97z1o44HPTg_rpEMyuS0s7uyZRF8OIE830AI130_provenance
{
dgn-np:NP383248.RAnvchppR97z1o44HPTg_rpEMyuS0s7uyZRF8OIE830AI130_assertion
dcterms:description
"[The unexpected presence of SPG4 gene mutations in patients with sporadic spastic paraplegia suggests that gene testing should be done in individuals with pure or complicated spastic paraplegia without family histories.]. 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:16055926
;
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:NP383248.RAnvchppR97z1o44HPTg_rpEMyuS0s7uyZRF8OIE830AI130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:48+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: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" .
}