@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" .
}