@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP1140379.RA0pnSu_TGU8gfr5swVNkWBQLKd8TcQ_wfCBsFOWz7x8w> .
@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:NP1140379.RA0pnSu_TGU8gfr5swVNkWBQLKd8TcQ_wfCBsFOWz7x8w130_head {
  this: np:hasAssertion dgn-np:NP1140379.RA0pnSu_TGU8gfr5swVNkWBQLKd8TcQ_wfCBsFOWz7x8w130_assertion;
    np:hasProvenance dgn-np:NP1140379.RA0pnSu_TGU8gfr5swVNkWBQLKd8TcQ_wfCBsFOWz7x8w130_provenance;
    np:hasPublicationInfo dgn-np:NP1140379.RA0pnSu_TGU8gfr5swVNkWBQLKd8TcQ_wfCBsFOWz7x8w130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP1140379.RA0pnSu_TGU8gfr5swVNkWBQLKd8TcQ_wfCBsFOWz7x8w130_assertion a np:Assertion .
  
  dgn-np:NP1140379.RA0pnSu_TGU8gfr5swVNkWBQLKd8TcQ_wfCBsFOWz7x8w130_provenance a np:Provenance .
  
  dgn-np:NP1140379.RA0pnSu_TGU8gfr5swVNkWBQLKd8TcQ_wfCBsFOWz7x8w130_publicationInfo
    a np:PublicationInfo .
}

dgn-np:NP1140379.RA0pnSu_TGU8gfr5swVNkWBQLKd8TcQ_wfCBsFOWz7x8w130_assertion {
  miriam-gene:257 a ncit:C16612 .
  
  lld:C1876203 a ncit:C7057 .
  
  dgn-gda:DGN14b67b803e2533e8221c4fef99c144a0 sio:SIO_000628 miriam-gene:257, lld:C1876203;
    a sio:SIO_001121 .
}

dgn-np:NP1140379.RA0pnSu_TGU8gfr5swVNkWBQLKd8TcQ_wfCBsFOWz7x8w130_provenance {
  dgn-np:NP1140379.RA0pnSu_TGU8gfr5swVNkWBQLKd8TcQ_wfCBsFOWz7x8w130_assertion dcterms:description
      "[Only a small number of genes have been associated with FND phenotypes until now, the first gene being EFNB1, related to craniofrontonasal syndrome (CFNS) with craniosynostosis in addition, and more recently the aristaless-like homeobox genes ALX3, ALX4, and ALX1, which have been related with distinct phenotypes named FND1, FND2, and FND3 respectively.]. 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:24376213;
    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:NP1140379.RA0pnSu_TGU8gfr5swVNkWBQLKd8TcQ_wfCBsFOWz7x8w130_publicationInfo {
  this: dcterms:created "2016-05-13T12:50:23+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" .
}