@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP482256.RAGmvavPm9t-pgGVNgs4RMCcqQzQ4C_hNNzsr7bVxxy1E> .
@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:NP482256.RAGmvavPm9t-pgGVNgs4RMCcqQzQ4C_hNNzsr7bVxxy1E130_head {
  this: np:hasAssertion dgn-np:NP482256.RAGmvavPm9t-pgGVNgs4RMCcqQzQ4C_hNNzsr7bVxxy1E130_assertion ;
    np:hasProvenance dgn-np:NP482256.RAGmvavPm9t-pgGVNgs4RMCcqQzQ4C_hNNzsr7bVxxy1E130_provenance ;
    np:hasPublicationInfo dgn-np:NP482256.RAGmvavPm9t-pgGVNgs4RMCcqQzQ4C_hNNzsr7bVxxy1E130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP482256.RAGmvavPm9t-pgGVNgs4RMCcqQzQ4C_hNNzsr7bVxxy1E130_assertion a np:Assertion .
  dgn-np:NP482256.RAGmvavPm9t-pgGVNgs4RMCcqQzQ4C_hNNzsr7bVxxy1E130_provenance a np:Provenance .
  dgn-np:NP482256.RAGmvavPm9t-pgGVNgs4RMCcqQzQ4C_hNNzsr7bVxxy1E130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP482256.RAGmvavPm9t-pgGVNgs4RMCcqQzQ4C_hNNzsr7bVxxy1E130_assertion {
  miriam-gene:3047 a ncit:C16612 .
  lld:C0472772 a ncit:C7057 .
  dgn-gda:DGN1914586a9a0d96a88f25dc4bb7dc2cd8 sio:SIO_000628 miriam-gene:3047 , lld:C0472772 ;
    a sio:SIO_001121 .
}
dgn-np:NP482256.RAGmvavPm9t-pgGVNgs4RMCcqQzQ4C_hNNzsr7bVxxy1E130_provenance {
  dgn-np:NP482256.RAGmvavPm9t-pgGVNgs4RMCcqQzQ4C_hNNzsr7bVxxy1E130_assertion dcterms:description "[Methodology suitable for such studies is reviewed, various abnormal fetal hemoglobins are discussed, the occurrence of Hb Bart's (gamma 4) and of the embryonic zeta chain is evaluated, and the various types of gamma-globin gene rearrangements (-A gamma.A gamma-; -G gamma.G gamma-; gamma-thalassemia; gamma-globin gene triplications, quadruplications, and quintuplications) are compared.]. 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:1802881 ;
    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:NP482256.RAGmvavPm9t-pgGVNgs4RMCcqQzQ4C_hNNzsr7bVxxy1E130_publicationInfo {
  this: dcterms:created "2014-10-02T12:36:48+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" .
}