@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP855113.RAQaGQYgMBGe2TI3IutN4s_YpebWzW3J6TWCo_OHXgPRg
> .
@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:NP855113.RAQaGQYgMBGe2TI3IutN4s_YpebWzW3J6TWCo_OHXgPRg130_head
{
this:
np:hasAssertion
dgn-np:NP855113.RAQaGQYgMBGe2TI3IutN4s_YpebWzW3J6TWCo_OHXgPRg130_assertion
;
np:hasProvenance
dgn-np:NP855113.RAQaGQYgMBGe2TI3IutN4s_YpebWzW3J6TWCo_OHXgPRg130_provenance
;
np:hasPublicationInfo
dgn-np:NP855113.RAQaGQYgMBGe2TI3IutN4s_YpebWzW3J6TWCo_OHXgPRg130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP855113.RAQaGQYgMBGe2TI3IutN4s_YpebWzW3J6TWCo_OHXgPRg130_assertion
a
np:Assertion
.
dgn-np:NP855113.RAQaGQYgMBGe2TI3IutN4s_YpebWzW3J6TWCo_OHXgPRg130_provenance
a
np:Provenance
.
dgn-np:NP855113.RAQaGQYgMBGe2TI3IutN4s_YpebWzW3J6TWCo_OHXgPRg130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP855113.RAQaGQYgMBGe2TI3IutN4s_YpebWzW3J6TWCo_OHXgPRg130_assertion
{
miriam-gene:3508
a
ncit:C16612
.
lld:C0393541
a
ncit:C7057
.
dgn-gda:DGN7ccd27548a42a7db12070a165d94f4e9
sio:SIO_000628
miriam-gene:3508
,
lld:C0393541
;
a
sio:SIO_001121
.
}
dgn-np:NP855113.RAQaGQYgMBGe2TI3IutN4s_YpebWzW3J6TWCo_OHXgPRg130_provenance
{
dgn-np:NP855113.RAQaGQYgMBGe2TI3IutN4s_YpebWzW3J6TWCo_OHXgPRg130_assertion
dcterms:description
"[The sequencing of IGHMBP2, the human homologue of the mouse neuromuscular degeneration gene (nmd) that accounts for spinal muscular atrophy with respiratory distress, failed to detect any mutation in our chronic distal spinal muscular atrophy patients, suggesting that spinal muscular atrophy with respiratory distress and chronic distal spinal muscular atrophy are caused by distinct genes located in the same chromosomal 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:12112104
;
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:NP855113.RAQaGQYgMBGe2TI3IutN4s_YpebWzW3J6TWCo_OHXgPRg130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:43+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" .
}