@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP924818.RA6TynF_vynRSzHIsfeRcgOW0HXzCNnDkSQU2H_byk-vQ
> .
@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:NP924818.RA6TynF_vynRSzHIsfeRcgOW0HXzCNnDkSQU2H_byk-vQ130_head
{
this:
np:hasAssertion
dgn-np:NP924818.RA6TynF_vynRSzHIsfeRcgOW0HXzCNnDkSQU2H_byk-vQ130_assertion
;
np:hasProvenance
dgn-np:NP924818.RA6TynF_vynRSzHIsfeRcgOW0HXzCNnDkSQU2H_byk-vQ130_provenance
;
np:hasPublicationInfo
dgn-np:NP924818.RA6TynF_vynRSzHIsfeRcgOW0HXzCNnDkSQU2H_byk-vQ130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP924818.RA6TynF_vynRSzHIsfeRcgOW0HXzCNnDkSQU2H_byk-vQ130_assertion
a
np:Assertion
.
dgn-np:NP924818.RA6TynF_vynRSzHIsfeRcgOW0HXzCNnDkSQU2H_byk-vQ130_provenance
a
np:Provenance
.
dgn-np:NP924818.RA6TynF_vynRSzHIsfeRcgOW0HXzCNnDkSQU2H_byk-vQ130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP924818.RA6TynF_vynRSzHIsfeRcgOW0HXzCNnDkSQU2H_byk-vQ130_assertion
{
miriam-gene:10561
a
ncit:C16612
.
lld:C0026847
a
ncit:C7057
.
dgn-gda:DGN018b9930b61099d393ac4c4516cc8aa2
sio:SIO_000628
miriam-gene:10561
,
lld:C0026847
;
a
sio:SIO_001121
.
}
dgn-np:NP924818.RA6TynF_vynRSzHIsfeRcgOW0HXzCNnDkSQU2H_byk-vQ130_provenance
{
dgn-np:NP924818.RA6TynF_vynRSzHIsfeRcgOW0HXzCNnDkSQU2H_byk-vQ130_assertion
dcterms:description
"[The spinal muscular atrophy candidate interval genes including survival motor neuron, the responsible gene in spinal muscular atrophy phenotype expression, neuronal apoptosis inhibitory protein, and P44, potential modifying genes, are located on chromosome 5q13 in two highly homologous copies (telomeric and centromeric) within the spinal muscular atrophy region.]. 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:17903057
;
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:NP924818.RA6TynF_vynRSzHIsfeRcgOW0HXzCNnDkSQU2H_byk-vQ130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:41:27+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" .
}