@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP735987.RA_hXvDuMdVypzUsyyXCXGvncGE84MpSkogfK2VQ_Ygyg
> .
@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:NP735987.RA_hXvDuMdVypzUsyyXCXGvncGE84MpSkogfK2VQ_Ygyg130_head
{
this:
np:hasAssertion
dgn-np:NP735987.RA_hXvDuMdVypzUsyyXCXGvncGE84MpSkogfK2VQ_Ygyg130_assertion
;
np:hasProvenance
dgn-np:NP735987.RA_hXvDuMdVypzUsyyXCXGvncGE84MpSkogfK2VQ_Ygyg130_provenance
;
np:hasPublicationInfo
dgn-np:NP735987.RA_hXvDuMdVypzUsyyXCXGvncGE84MpSkogfK2VQ_Ygyg130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP735987.RA_hXvDuMdVypzUsyyXCXGvncGE84MpSkogfK2VQ_Ygyg130_assertion
a
np:Assertion
.
dgn-np:NP735987.RA_hXvDuMdVypzUsyyXCXGvncGE84MpSkogfK2VQ_Ygyg130_provenance
a
np:Provenance
.
dgn-np:NP735987.RA_hXvDuMdVypzUsyyXCXGvncGE84MpSkogfK2VQ_Ygyg130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP735987.RA_hXvDuMdVypzUsyyXCXGvncGE84MpSkogfK2VQ_Ygyg130_assertion
{
miriam-gene:6607
a
ncit:C16612
.
lld:C0026846
a
ncit:C7057
.
dgn-gda:DGNf0c79c920f7adf5780359b3802ab1073
sio:SIO_000628
miriam-gene:6607
,
lld:C0026846
;
a
sio:SIO_001121
.
}
dgn-np:NP735987.RA_hXvDuMdVypzUsyyXCXGvncGE84MpSkogfK2VQ_Ygyg130_provenance
{
dgn-np:NP735987.RA_hXvDuMdVypzUsyyXCXGvncGE84MpSkogfK2VQ_Ygyg130_assertion
dcterms:description
"[The disease is caused by loss of the survival of motoneuron (SMN) protein, resulting in the degeneration of alpha motoneurons in spinal cord and muscular atrophy in the limbs and trunk.]. 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:21956898
;
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:NP735987.RA_hXvDuMdVypzUsyyXCXGvncGE84MpSkogfK2VQ_Ygyg130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:26+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" .
}