@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP1399660.RAgY3VJ8l5R_MVCVxfHWL6woP_rL8aO5UkwhbJ7P0TvnI
> .
@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/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@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/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v4.0.0/void/
> .
dgn-np:NP1399660.RAgY3VJ8l5R_MVCVxfHWL6woP_rL8aO5UkwhbJ7P0TvnI130_head
{
this:
np:hasAssertion
dgn-np:NP1399660.RAgY3VJ8l5R_MVCVxfHWL6woP_rL8aO5UkwhbJ7P0TvnI130_assertion
;
np:hasProvenance
dgn-np:NP1399660.RAgY3VJ8l5R_MVCVxfHWL6woP_rL8aO5UkwhbJ7P0TvnI130_provenance
;
np:hasPublicationInfo
dgn-np:NP1399660.RAgY3VJ8l5R_MVCVxfHWL6woP_rL8aO5UkwhbJ7P0TvnI130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP1399660.RAgY3VJ8l5R_MVCVxfHWL6woP_rL8aO5UkwhbJ7P0TvnI130_assertion
a
np:Assertion
.
dgn-np:NP1399660.RAgY3VJ8l5R_MVCVxfHWL6woP_rL8aO5UkwhbJ7P0TvnI130_provenance
a
np:Provenance
.
dgn-np:NP1399660.RAgY3VJ8l5R_MVCVxfHWL6woP_rL8aO5UkwhbJ7P0TvnI130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP1399660.RAgY3VJ8l5R_MVCVxfHWL6woP_rL8aO5UkwhbJ7P0TvnI130_assertion
{
miriam-gene:4671
a
ncit:C16612
.
lld:C0026847
a
ncit:C7057
.
dgn-gda:DGN13d77709d2dc439b9931032c75548a4b
sio:SIO_000628
miriam-gene:4671
,
lld:C0026847
;
a
sio:SIO_001121
.
}
dgn-np:NP1399660.RAgY3VJ8l5R_MVCVxfHWL6woP_rL8aO5UkwhbJ7P0TvnI130_provenance
{
dgn-np:NP1399660.RAgY3VJ8l5R_MVCVxfHWL6woP_rL8aO5UkwhbJ7P0TvnI130_assertion
dcterms:description
"[Our results show that the incidence of NAIP deletion is higher in the more severe SMA cases and the dual deletions of the SMN and NAIP genes are more common in Saudi SMA type-I patients compared to patients of other ethnic groups.]. 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:9667776
;
prov:wasDerivedFrom
dgn-void:befree-2016
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-2016
pav:importedOn
"2016-02-19"^^
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:NP1399660.RAgY3VJ8l5R_MVCVxfHWL6woP_rL8aO5UkwhbJ7P0TvnI130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:52:20+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:disgenetv3.0rdf
;
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
"v4.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v4.0.0" .
}