@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP1367716.RAo56Ialq_pDqhwi8aqGDmuE6aLoeaGr3fkVWWBok9CvE> .
@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:NP1367716.RAo56Ialq_pDqhwi8aqGDmuE6aLoeaGr3fkVWWBok9CvE130_head {
  this: np:hasAssertion dgn-np:NP1367716.RAo56Ialq_pDqhwi8aqGDmuE6aLoeaGr3fkVWWBok9CvE130_assertion;
    np:hasProvenance dgn-np:NP1367716.RAo56Ialq_pDqhwi8aqGDmuE6aLoeaGr3fkVWWBok9CvE130_provenance;
    np:hasPublicationInfo dgn-np:NP1367716.RAo56Ialq_pDqhwi8aqGDmuE6aLoeaGr3fkVWWBok9CvE130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP1367716.RAo56Ialq_pDqhwi8aqGDmuE6aLoeaGr3fkVWWBok9CvE130_assertion a np:Assertion .
  
  dgn-np:NP1367716.RAo56Ialq_pDqhwi8aqGDmuE6aLoeaGr3fkVWWBok9CvE130_provenance a np:Provenance .
  
  dgn-np:NP1367716.RAo56Ialq_pDqhwi8aqGDmuE6aLoeaGr3fkVWWBok9CvE130_publicationInfo
    a np:PublicationInfo .
}

dgn-np:NP1367716.RAo56Ialq_pDqhwi8aqGDmuE6aLoeaGr3fkVWWBok9CvE130_assertion {
  miriam-gene:3908 a ncit:C16612 .
  
  lld:C0699743 a ncit:C7057 .
  
  dgn-gda:DGN9006896ab93628f07931ef1769696243 sio:SIO_000628 miriam-gene:3908, lld:C0699743;
    a sio:SIO_001121 .
}

dgn-np:NP1367716.RAo56Ialq_pDqhwi8aqGDmuE6aLoeaGr3fkVWWBok9CvE130_provenance {
  dgn-np:NP1367716.RAo56Ialq_pDqhwi8aqGDmuE6aLoeaGr3fkVWWBok9CvE130_assertion dcterms:description
      "[About half of the children with classical congenital muscular dystrophy (CMD) show an absence in their skeletal muscle of laminin alpha2 chain, one of the components of the extracellular matrix protein, merosin.]. 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:9039983;
    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:NP1367716.RAo56Ialq_pDqhwi8aqGDmuE6aLoeaGr3fkVWWBok9CvE130_publicationInfo {
  this: dcterms:created "2016-05-13T12:52:06+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" .
}