@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP154244.RAsWEAR_vVsq-HF-FM0Bs5Oab-Bbs4DuHBAJORjK-2Ieo> .
@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:NP154244.RAsWEAR_vVsq-HF-FM0Bs5Oab-Bbs4DuHBAJORjK-2Ieo130_head {
  this: np:hasAssertion dgn-np:NP154244.RAsWEAR_vVsq-HF-FM0Bs5Oab-Bbs4DuHBAJORjK-2Ieo130_assertion;
    np:hasProvenance dgn-np:NP154244.RAsWEAR_vVsq-HF-FM0Bs5Oab-Bbs4DuHBAJORjK-2Ieo130_provenance;
    np:hasPublicationInfo dgn-np:NP154244.RAsWEAR_vVsq-HF-FM0Bs5Oab-Bbs4DuHBAJORjK-2Ieo130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP154244.RAsWEAR_vVsq-HF-FM0Bs5Oab-Bbs4DuHBAJORjK-2Ieo130_assertion a np:Assertion .
  
  dgn-np:NP154244.RAsWEAR_vVsq-HF-FM0Bs5Oab-Bbs4DuHBAJORjK-2Ieo130_provenance a np:Provenance .
  
  dgn-np:NP154244.RAsWEAR_vVsq-HF-FM0Bs5Oab-Bbs4DuHBAJORjK-2Ieo130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP154244.RAsWEAR_vVsq-HF-FM0Bs5Oab-Bbs4DuHBAJORjK-2Ieo130_assertion {
  miriam-gene:2477 a ncit:C16612 .
  
  lld:C0235031 a ncit:C7057 .
  
  dgn-gda:DGN21df130da79430b01b5f87008073ccd0 sio:SIO_000628 miriam-gene:2477, lld:C0235031;
    a sio:SIO_001121 .
}

dgn-np:NP154244.RAsWEAR_vVsq-HF-FM0Bs5Oab-Bbs4DuHBAJORjK-2Ieo130_provenance {
  dgn-np:NP154244.RAsWEAR_vVsq-HF-FM0Bs5Oab-Bbs4DuHBAJORjK-2Ieo130_assertion dcterms:description
      "[Should an FMR1 premutation be uncovered, this will allow patients to make informed reproductive decisions and help clinicians to properly diagnose family members who may have menstrual irregularity, developmental delay, or neurologic symptoms.]. 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:16275254;
    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:NP154244.RAsWEAR_vVsq-HF-FM0Bs5Oab-Bbs4DuHBAJORjK-2Ieo130_publicationInfo {
  this: dcterms:created "2014-10-02T12:33:22+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" .
}