@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP830175.RA6CL-qNrT_35__2jUQAbPPqXv7bFwAFuxRouulP18-WM> .
@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:NP830175.RA6CL-qNrT_35__2jUQAbPPqXv7bFwAFuxRouulP18-WM130_head {
  this: np:hasAssertion dgn-np:NP830175.RA6CL-qNrT_35__2jUQAbPPqXv7bFwAFuxRouulP18-WM130_assertion ;
    np:hasProvenance dgn-np:NP830175.RA6CL-qNrT_35__2jUQAbPPqXv7bFwAFuxRouulP18-WM130_provenance ;
    np:hasPublicationInfo dgn-np:NP830175.RA6CL-qNrT_35__2jUQAbPPqXv7bFwAFuxRouulP18-WM130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP830175.RA6CL-qNrT_35__2jUQAbPPqXv7bFwAFuxRouulP18-WM130_assertion a np:Assertion .
  dgn-np:NP830175.RA6CL-qNrT_35__2jUQAbPPqXv7bFwAFuxRouulP18-WM130_provenance a np:Provenance .
  dgn-np:NP830175.RA6CL-qNrT_35__2jUQAbPPqXv7bFwAFuxRouulP18-WM130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP830175.RA6CL-qNrT_35__2jUQAbPPqXv7bFwAFuxRouulP18-WM130_assertion {
  miriam-gene:3483 a ncit:C16612 .
  lld:C0013336 a ncit:C7057 .
  dgn-gda:DGNbb29c4ee1654bc2c98864b58f48ef274 sio:SIO_000628 miriam-gene:3483 , lld:C0013336 ;
    a sio:SIO_001121 .
}
dgn-np:NP830175.RA6CL-qNrT_35__2jUQAbPPqXv7bFwAFuxRouulP18-WM130_provenance {
  dgn-np:NP830175.RA6CL-qNrT_35__2jUQAbPPqXv7bFwAFuxRouulP18-WM130_assertion dcterms:description "[The observation that in families of ALS deficient patients, heterozygous carriers for IGFALS gene mutations are shorter than their wild type relatives and the relatively high frequency of heterozygosity for this gene in children with idiopathic short stature suggests a requirement of normal levels of ALS for the attainment of maximal growth potential.]. 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:20679994 ;
    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:NP830175.RA6CL-qNrT_35__2jUQAbPPqXv7bFwAFuxRouulP18-WM130_publicationInfo {
  this: dcterms:created "2016-05-13T12:48:01+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" .
}