@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP682465.RAGcT0ekFyjGbbaTUqPQeYFwndQy4nS91fZR-wgMx5etQ
> .
@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:NP682465.RAGcT0ekFyjGbbaTUqPQeYFwndQy4nS91fZR-wgMx5etQ130_head
{
this:
np:hasAssertion
dgn-np:NP682465.RAGcT0ekFyjGbbaTUqPQeYFwndQy4nS91fZR-wgMx5etQ130_assertion
;
np:hasProvenance
dgn-np:NP682465.RAGcT0ekFyjGbbaTUqPQeYFwndQy4nS91fZR-wgMx5etQ130_provenance
;
np:hasPublicationInfo
dgn-np:NP682465.RAGcT0ekFyjGbbaTUqPQeYFwndQy4nS91fZR-wgMx5etQ130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP682465.RAGcT0ekFyjGbbaTUqPQeYFwndQy4nS91fZR-wgMx5etQ130_assertion
a
np:Assertion
.
dgn-np:NP682465.RAGcT0ekFyjGbbaTUqPQeYFwndQy4nS91fZR-wgMx5etQ130_provenance
a
np:Provenance
.
dgn-np:NP682465.RAGcT0ekFyjGbbaTUqPQeYFwndQy4nS91fZR-wgMx5etQ130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP682465.RAGcT0ekFyjGbbaTUqPQeYFwndQy4nS91fZR-wgMx5etQ130_assertion
{
miriam-gene:6638
a
ncit:C16612
.
lld:C0026847
a
ncit:C7057
.
dgn-gda:DGNa9871db728416d48485e5993b6dc581e
sio:SIO_000628
miriam-gene:6638
,
lld:C0026847
;
a
sio:SIO_001121
.
}
dgn-np:NP682465.RAGcT0ekFyjGbbaTUqPQeYFwndQy4nS91fZR-wgMx5etQ130_provenance
{
dgn-np:NP682465.RAGcT0ekFyjGbbaTUqPQeYFwndQy4nS91fZR-wgMx5etQ130_assertion
dcterms:description
"[It is also supposed that individually variable levels of SMN protein, together with influences of other phenotype modifier genes and their products, cause the clinical SMA spectrum through differential degree of motoneuron functional loss.]. 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:18629520
;
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:NP682465.RAGcT0ekFyjGbbaTUqPQeYFwndQy4nS91fZR-wgMx5etQ130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:46:54+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" .
}