@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP262557.RAW9nwM4NXZEjyfR9pQfBD7nh3d6X77cPSCtAWx5v0tJI
> .
@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:NP262557.RAW9nwM4NXZEjyfR9pQfBD7nh3d6X77cPSCtAWx5v0tJI130_head
{
this:
np:hasAssertion
dgn-np:NP262557.RAW9nwM4NXZEjyfR9pQfBD7nh3d6X77cPSCtAWx5v0tJI130_assertion
;
np:hasProvenance
dgn-np:NP262557.RAW9nwM4NXZEjyfR9pQfBD7nh3d6X77cPSCtAWx5v0tJI130_provenance
;
np:hasPublicationInfo
dgn-np:NP262557.RAW9nwM4NXZEjyfR9pQfBD7nh3d6X77cPSCtAWx5v0tJI130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP262557.RAW9nwM4NXZEjyfR9pQfBD7nh3d6X77cPSCtAWx5v0tJI130_assertion
a
np:Assertion
.
dgn-np:NP262557.RAW9nwM4NXZEjyfR9pQfBD7nh3d6X77cPSCtAWx5v0tJI130_provenance
a
np:Provenance
.
dgn-np:NP262557.RAW9nwM4NXZEjyfR9pQfBD7nh3d6X77cPSCtAWx5v0tJI130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP262557.RAW9nwM4NXZEjyfR9pQfBD7nh3d6X77cPSCtAWx5v0tJI130_assertion
{
miriam-gene:8487
a
ncit:C16612
.
lld:C0085084
a
ncit:C7057
.
dgn-gda:DGN1db0427a1d5943ceb378aa602420ef2d
sio:SIO_000628
miriam-gene:8487
,
lld:C0085084
;
a
sio:SIO_001121
.
}
dgn-np:NP262557.RAW9nwM4NXZEjyfR9pQfBD7nh3d6X77cPSCtAWx5v0tJI130_provenance
{
dgn-np:NP262557.RAW9nwM4NXZEjyfR9pQfBD7nh3d6X77cPSCtAWx5v0tJI130_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:NP262557.RAW9nwM4NXZEjyfR9pQfBD7nh3d6X77cPSCtAWx5v0tJI130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:26+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: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" .
}