@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP875407.RAA8uqiyGiLsippLZvVNGA4zKGUzQT1y7F9UacSIFyXb4
> .
@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:NP875407.RAA8uqiyGiLsippLZvVNGA4zKGUzQT1y7F9UacSIFyXb4130_head
{
this:
np:hasAssertion
dgn-np:NP875407.RAA8uqiyGiLsippLZvVNGA4zKGUzQT1y7F9UacSIFyXb4130_assertion
;
np:hasProvenance
dgn-np:NP875407.RAA8uqiyGiLsippLZvVNGA4zKGUzQT1y7F9UacSIFyXb4130_provenance
;
np:hasPublicationInfo
dgn-np:NP875407.RAA8uqiyGiLsippLZvVNGA4zKGUzQT1y7F9UacSIFyXb4130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP875407.RAA8uqiyGiLsippLZvVNGA4zKGUzQT1y7F9UacSIFyXb4130_assertion
a
np:Assertion
.
dgn-np:NP875407.RAA8uqiyGiLsippLZvVNGA4zKGUzQT1y7F9UacSIFyXb4130_provenance
a
np:Provenance
.
dgn-np:NP875407.RAA8uqiyGiLsippLZvVNGA4zKGUzQT1y7F9UacSIFyXb4130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP875407.RAA8uqiyGiLsippLZvVNGA4zKGUzQT1y7F9UacSIFyXb4130_assertion
{
miriam-gene:9839
a
ncit:C16612
.
lld:C0026847
a
ncit:C7057
.
dgn-gda:DGN1a2c9f9b011b0e5b477faab8fe3ecbe0
sio:SIO_000628
miriam-gene:9839
,
lld:C0026847
;
a
sio:SIO_001121
.
}
dgn-np:NP875407.RAA8uqiyGiLsippLZvVNGA4zKGUzQT1y7F9UacSIFyXb4130_provenance
{
dgn-np:NP875407.RAA8uqiyGiLsippLZvVNGA4zKGUzQT1y7F9UacSIFyXb4130_assertion
dcterms:description
"[These findings suggest that an aberrant alternative splicing event in SIP1 occurs tissues derived from patients with the motor neuron diseases, and contributes to the pathological process of SMA and ALS.]. 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:11943600
;
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:NP875407.RAA8uqiyGiLsippLZvVNGA4zKGUzQT1y7F9UacSIFyXb4130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:55+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" .
}