@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP628734.RAMhJwqKr3akijK5xd0UtsGeUhoiJ4vm9e7anLS2yWXug> .
@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:NP628734.RAMhJwqKr3akijK5xd0UtsGeUhoiJ4vm9e7anLS2yWXug130_head {
  this: np:hasAssertion dgn-np:NP628734.RAMhJwqKr3akijK5xd0UtsGeUhoiJ4vm9e7anLS2yWXug130_assertion;
    np:hasProvenance dgn-np:NP628734.RAMhJwqKr3akijK5xd0UtsGeUhoiJ4vm9e7anLS2yWXug130_provenance;
    np:hasPublicationInfo dgn-np:NP628734.RAMhJwqKr3akijK5xd0UtsGeUhoiJ4vm9e7anLS2yWXug130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP628734.RAMhJwqKr3akijK5xd0UtsGeUhoiJ4vm9e7anLS2yWXug130_assertion a np:Assertion .
  
  dgn-np:NP628734.RAMhJwqKr3akijK5xd0UtsGeUhoiJ4vm9e7anLS2yWXug130_provenance a np:Provenance .
  
  dgn-np:NP628734.RAMhJwqKr3akijK5xd0UtsGeUhoiJ4vm9e7anLS2yWXug130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP628734.RAMhJwqKr3akijK5xd0UtsGeUhoiJ4vm9e7anLS2yWXug130_assertion {
  miriam-gene:3915 a ncit:C16612 .
  
  lld:C0027726 a ncit:C7057 .
  
  dgn-gda:DGN680b2b523957cc57fd0b8bf6e4f56575 sio:SIO_000628 miriam-gene:3915, lld:C0027726;
    a sio:SIO_001121 .
}

dgn-np:NP628734.RAMhJwqKr3akijK5xd0UtsGeUhoiJ4vm9e7anLS2yWXug130_provenance {
  dgn-np:NP628734.RAMhJwqKr3akijK5xd0UtsGeUhoiJ4vm9e7anLS2yWXug130_assertion dcterms:description
      "[Because of its prognostic relevance, we advocate molecular genetic testing of LAMB2 in any case of prenatally detected nephrotic syndrome with negative results of NPHS1 mutational screening, especially in the presence of the typical sonomorphologic findings of the kidneys and the development of oligohydramnios.]. 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:16450351;
    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:NP628734.RAMhJwqKr3akijK5xd0UtsGeUhoiJ4vm9e7anLS2yWXug130_publicationInfo {
  this: dcterms:created "2014-10-02T12:38:19+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" .
}