@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP527008.RAmWkKevoi0OZDSxyvwwuhJrIJslTYj2mQchaVT6gm3dg> .
@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:NP527008.RAmWkKevoi0OZDSxyvwwuhJrIJslTYj2mQchaVT6gm3dg130_head {
  this: np:hasAssertion dgn-np:NP527008.RAmWkKevoi0OZDSxyvwwuhJrIJslTYj2mQchaVT6gm3dg130_assertion ;
    np:hasProvenance dgn-np:NP527008.RAmWkKevoi0OZDSxyvwwuhJrIJslTYj2mQchaVT6gm3dg130_provenance ;
    np:hasPublicationInfo dgn-np:NP527008.RAmWkKevoi0OZDSxyvwwuhJrIJslTYj2mQchaVT6gm3dg130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP527008.RAmWkKevoi0OZDSxyvwwuhJrIJslTYj2mQchaVT6gm3dg130_assertion a np:Assertion .
  dgn-np:NP527008.RAmWkKevoi0OZDSxyvwwuhJrIJslTYj2mQchaVT6gm3dg130_provenance a np:Provenance .
  dgn-np:NP527008.RAmWkKevoi0OZDSxyvwwuhJrIJslTYj2mQchaVT6gm3dg130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP527008.RAmWkKevoi0OZDSxyvwwuhJrIJslTYj2mQchaVT6gm3dg130_assertion {
  miriam-gene:147495 a ncit:C16612 .
  lld:C0030312 a ncit:C7057 .
  dgn-gda:DGNb8c91b6a73e3540eb10a62cf25a8ff91 sio:SIO_000628 miriam-gene:147495 , lld:C0030312 ;
    a sio:SIO_001121 .
}
dgn-np:NP527008.RAmWkKevoi0OZDSxyvwwuhJrIJslTYj2mQchaVT6gm3dg130_provenance {
  dgn-np:NP527008.RAmWkKevoi0OZDSxyvwwuhJrIJslTYj2mQchaVT6gm3dg130_assertion dcterms:description "[In addition to the previously described important signs of HHS, i.e., prenatal growth retardation, microcephaly, psychomotor retardation, progressive pancytopenia, immunological abnormalities, and cerebellar hypoplasia and ataxia, we consider that delayed myelination of cerebral white matter and hypoplastic corpus callosum should be added to the list of important signs.]. 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:10963101 ;
    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:NP527008.RAmWkKevoi0OZDSxyvwwuhJrIJslTYj2mQchaVT6gm3dg130_publicationInfo {
  this: dcterms:created "2014-10-02T12:37:16+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" .
}