@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP328668.RAgSjCxiZkwyr9xHWwvFJP19lLsioCm73iPPXtNawjNjM
> .
@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:NP328668.RAgSjCxiZkwyr9xHWwvFJP19lLsioCm73iPPXtNawjNjM130_head
{
this:
np:hasAssertion
dgn-np:NP328668.RAgSjCxiZkwyr9xHWwvFJP19lLsioCm73iPPXtNawjNjM130_assertion
;
np:hasProvenance
dgn-np:NP328668.RAgSjCxiZkwyr9xHWwvFJP19lLsioCm73iPPXtNawjNjM130_provenance
;
np:hasPublicationInfo
dgn-np:NP328668.RAgSjCxiZkwyr9xHWwvFJP19lLsioCm73iPPXtNawjNjM130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP328668.RAgSjCxiZkwyr9xHWwvFJP19lLsioCm73iPPXtNawjNjM130_assertion
a
np:Assertion
.
dgn-np:NP328668.RAgSjCxiZkwyr9xHWwvFJP19lLsioCm73iPPXtNawjNjM130_provenance
a
np:Provenance
.
dgn-np:NP328668.RAgSjCxiZkwyr9xHWwvFJP19lLsioCm73iPPXtNawjNjM130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP328668.RAgSjCxiZkwyr9xHWwvFJP19lLsioCm73iPPXtNawjNjM130_assertion
{
miriam-gene:6606
a
ncit:C16612
.
lld:C0026847
a
ncit:C7057
.
dgn-gda:DGN6abddbb7de2a3d88a45ec26b016fa90a
sio:SIO_000628
miriam-gene:6606
,
lld:C0026847
;
a
sio:SIO_001121
.
}
dgn-np:NP328668.RAgSjCxiZkwyr9xHWwvFJP19lLsioCm73iPPXtNawjNjM130_provenance
{
dgn-np:NP328668.RAgSjCxiZkwyr9xHWwvFJP19lLsioCm73iPPXtNawjNjM130_assertion
dcterms:description
"[Our results show that IGHMBP2 is the second gene found to be defective in spinal muscular atrophy, and indicate that IGHMBP2 and SMN share common functions important for motor neuron maintenance and integrity in mammals.]. 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:11528396
;
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:NP328668.RAgSjCxiZkwyr9xHWwvFJP19lLsioCm73iPPXtNawjNjM130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:44:14+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" .
}