@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP648916.RAlKVdPqS7XP4ye9n2-D6VdXw4Yn-lZDFTujEuNAy28zs> .
@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:NP648916.RAlKVdPqS7XP4ye9n2-D6VdXw4Yn-lZDFTujEuNAy28zs130_head {
  this: np:hasAssertion dgn-np:NP648916.RAlKVdPqS7XP4ye9n2-D6VdXw4Yn-lZDFTujEuNAy28zs130_assertion;
    np:hasProvenance dgn-np:NP648916.RAlKVdPqS7XP4ye9n2-D6VdXw4Yn-lZDFTujEuNAy28zs130_provenance;
    np:hasPublicationInfo dgn-np:NP648916.RAlKVdPqS7XP4ye9n2-D6VdXw4Yn-lZDFTujEuNAy28zs130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP648916.RAlKVdPqS7XP4ye9n2-D6VdXw4Yn-lZDFTujEuNAy28zs130_assertion a np:Assertion .
  
  dgn-np:NP648916.RAlKVdPqS7XP4ye9n2-D6VdXw4Yn-lZDFTujEuNAy28zs130_provenance a np:Provenance .
  
  dgn-np:NP648916.RAlKVdPqS7XP4ye9n2-D6VdXw4Yn-lZDFTujEuNAy28zs130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP648916.RAlKVdPqS7XP4ye9n2-D6VdXw4Yn-lZDFTujEuNAy28zs130_assertion {
  miriam-gene:8048 a ncit:C16612 .
  
  lld:C0158646 a ncit:C7057 .
  
  dgn-gda:DGN3f3d264c093148ad345032ac6d66f5cb sio:SIO_000628 miriam-gene:8048, lld:C0158646;
    a sio:SIO_001121 .
}

dgn-np:NP648916.RAlKVdPqS7XP4ye9n2-D6VdXw4Yn-lZDFTujEuNAy28zs130_provenance {
  dgn-np:NP648916.RAlKVdPqS7XP4ye9n2-D6VdXw4Yn-lZDFTujEuNAy28zs130_assertion dcterms:description
      "[Combining the results of chromosomal linkage studies of unidentified human CLP genes with insights from the mouse models, the following previously unexamined genes are identified as strong candidate genes for causative roles in human nonsyndromic CLP: BMP4, BMPR1B, TFAP2A, SOX4, WNT9B, WNT3, and SP8.]. 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:18181213;
    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:NP648916.RAlKVdPqS7XP4ye9n2-D6VdXw4Yn-lZDFTujEuNAy28zs130_publicationInfo {
  this: dcterms:created "2016-05-13T12:46:39+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" .
}