@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP571830.RAAQuMZCe_aACZ92RPW4KsCfDOJsBl1ABm8Qfm9vpM_pI> .
@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/v3.0.0/void/> .
dgn-np:NP571830.RAAQuMZCe_aACZ92RPW4KsCfDOJsBl1ABm8Qfm9vpM_pI130_head {
   this: np:hasAssertion dgn-np:NP571830.RAAQuMZCe_aACZ92RPW4KsCfDOJsBl1ABm8Qfm9vpM_pI130_assertion ;
    np:hasProvenance dgn-np:NP571830.RAAQuMZCe_aACZ92RPW4KsCfDOJsBl1ABm8Qfm9vpM_pI130_provenance ;
    np:hasPublicationInfo dgn-np:NP571830.RAAQuMZCe_aACZ92RPW4KsCfDOJsBl1ABm8Qfm9vpM_pI130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP571830.RAAQuMZCe_aACZ92RPW4KsCfDOJsBl1ABm8Qfm9vpM_pI130_assertion a np:Assertion .
  dgn-np:NP571830.RAAQuMZCe_aACZ92RPW4KsCfDOJsBl1ABm8Qfm9vpM_pI130_provenance a np:Provenance .
  dgn-np:NP571830.RAAQuMZCe_aACZ92RPW4KsCfDOJsBl1ABm8Qfm9vpM_pI130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP571830.RAAQuMZCe_aACZ92RPW4KsCfDOJsBl1ABm8Qfm9vpM_pI130_assertion {
   miriam-gene:4488 a ncit:C16612 .
  lld:C1837217 a ncit:C7057 .
  dgn-gda:DGNcf22c65dc7b4d32687418d37fbe81021 sio:SIO_000628 miriam-gene:4488 , lld:C1837217 ;
    a sio:SIO_001121 .
}
dgn-np:NP571830.RAAQuMZCe_aACZ92RPW4KsCfDOJsBl1ABm8Qfm9vpM_pI130_provenance {
   dgn-np:NP571830.RAAQuMZCe_aACZ92RPW4KsCfDOJsBl1ABm8Qfm9vpM_pI130_assertion dcterms:description "[Sequence analysis alone suggests that point mutations in FOXE1, GLI2, JAG2, LHX8, MSX1, MSX2, SATB2, SKI, SPRY2, and TBX10 may be rare causes of isolated cleft lip with or without cleft palate, and the linkage disequilibrium data support a larger, as yet unspecified, role for variants in or near MSX2, JAG2, and SKI.]. 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:16327884 ;
    prov:wasDerivedFrom dgn-void:befree-20150227 ;
    prov:wasGeneratedBy eco:ECO_0000203 .
  dgn-void:befree-20150227 pav:importedOn "2015-02-27"^^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:NP571830.RAAQuMZCe_aACZ92RPW4KsCfDOJsBl1ABm8Qfm9vpM_pI130_publicationInfo {
   this: dcterms:created "2015-08-25T14:43:20+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 "v3.0.0.0" .
  dgn-void:disgenetv3.0rdf pav:version "v3.0.0" .
}