[ {
  "@graph" : [ {
    "@id" : "http://identifiers.org/ncbigene/139818",
    "@type" : [ "http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C16612" ]
  }, {
    "@id" : "http://linkedlifedata.com/resource/umls/id/C1850554",
    "@type" : [ "http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C7057" ]
  }, {
    "@id" : "http://rdf.disgenet.org/gene-disease-association.ttl#DGN1b296b10e823b4ad1dc6c76e259b7d91",
    "@type" : [ "http://semanticscience.org/resource/SIO_001121" ],
    "http://semanticscience.org/resource/SIO_000628" : [ {
      "@id" : "http://identifiers.org/ncbigene/139818"
    }, {
      "@id" : "http://linkedlifedata.com/resource/umls/id/C1850554"
    } ]
  } ],
  "@id" : "http://rdf.disgenet.org/nanopublications.trig#NP680334.RA3kYaeiZMf6vKtXzv0QF_tT88LSz9zoKkc6VYpaCXAVo130_assertion"
}, {
  "@graph" : [ {
    "@id" : "http://rdf.disgenet.org/nanopublications.trig#NP680334.RA3kYaeiZMf6vKtXzv0QF_tT88LSz9zoKkc6VYpaCXAVo",
    "@type" : [ "http://www.nanopub.org/nschema#Nanopublication" ],
    "http://www.nanopub.org/nschema#hasAssertion" : [ {
      "@id" : "http://rdf.disgenet.org/nanopublications.trig#NP680334.RA3kYaeiZMf6vKtXzv0QF_tT88LSz9zoKkc6VYpaCXAVo130_assertion"
    } ],
    "http://www.nanopub.org/nschema#hasProvenance" : [ {
      "@id" : "http://rdf.disgenet.org/nanopublications.trig#NP680334.RA3kYaeiZMf6vKtXzv0QF_tT88LSz9zoKkc6VYpaCXAVo130_provenance"
    } ],
    "http://www.nanopub.org/nschema#hasPublicationInfo" : [ {
      "@id" : "http://rdf.disgenet.org/nanopublications.trig#NP680334.RA3kYaeiZMf6vKtXzv0QF_tT88LSz9zoKkc6VYpaCXAVo130_publicationInfo"
    } ]
  }, {
    "@id" : "http://rdf.disgenet.org/nanopublications.trig#NP680334.RA3kYaeiZMf6vKtXzv0QF_tT88LSz9zoKkc6VYpaCXAVo130_assertion",
    "@type" : [ "http://www.nanopub.org/nschema#Assertion" ]
  }, {
    "@id" : "http://rdf.disgenet.org/nanopublications.trig#NP680334.RA3kYaeiZMf6vKtXzv0QF_tT88LSz9zoKkc6VYpaCXAVo130_provenance",
    "@type" : [ "http://www.nanopub.org/nschema#Provenance" ]
  }, {
    "@id" : "http://rdf.disgenet.org/nanopublications.trig#NP680334.RA3kYaeiZMf6vKtXzv0QF_tT88LSz9zoKkc6VYpaCXAVo130_publicationInfo",
    "@type" : [ "http://www.nanopub.org/nschema#PublicationInfo" ]
  } ],
  "@id" : "http://rdf.disgenet.org/nanopublications.trig#NP680334.RA3kYaeiZMf6vKtXzv0QF_tT88LSz9zoKkc6VYpaCXAVo130_head"
}, {
  "@graph" : [ {
    "@id" : "http://rdf.disgenet.org/nanopublications.trig#NP680334.RA3kYaeiZMf6vKtXzv0QF_tT88LSz9zoKkc6VYpaCXAVo130_assertion",
    "http://purl.org/dc/terms/description" : [ {
      "@language" : "en",
      "@value" : "[When the sulfate transport function of the different DTDST mutations are grouped according to the general phenotypes, individuals with the most severe form, ACG-1B, tend to be homozygous for null mutations, individuals with the moderately severe atelosteogenesis type 2 have at least one allele with a loss-of-function mutation, and individuals with the mildest forms are typically homozygous for mutations with residual sulfate transport function.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."
    } ],
    "http://purl.org/ontology/wi/core#evidence" : [ {
      "@id" : "http://rdf.disgenet.org/v2.1.0/void.ttl#source_evidence_literature"
    } ],
    "http://semanticscience.org/resource/SIO_000772" : [ {
      "@id" : "http://identifiers.org/pubmed/11448940"
    } ],
    "http://www.w3.org/ns/prov#wasDerivedFrom" : [ {
      "@id" : "http://rdf.disgenet.org/v2.1.0/void.ttl#befree-20140225"
    } ],
    "http://www.w3.org/ns/prov#wasGeneratedBy" : [ {
      "@id" : "http://purl.obolibrary.org/obo/eco.owl#ECO_0000203"
    } ]
  }, {
    "@id" : "http://rdf.disgenet.org/v2.1.0/void.ttl#befree-20140225",
    "http://purl.org/pav/2.0/importedOn" : [ {
      "@type" : "http://www.w3.org/2001/XMLSchema#date",
      "@value" : "2014-02-25"
    } ]
  }, {
    "@id" : "http://rdf.disgenet.org/v2.1.0/void.ttl#source_evidence_literature",
    "@type" : [ "http://purl.obolibrary.org/obo/eco.owl#ECO_0000212" ],
    "http://www.w3.org/2000/01/rdf-schema#comment" : [ {
      "@language" : "en",
      "@value" : "Gene-disease associations inferred from text-mining the literature."
    } ],
    "http://www.w3.org/2000/01/rdf-schema#label" : [ {
      "@language" : "en",
      "@value" : "DisGeNET evidence - LITERATURE"
    } ]
  } ],
  "@id" : "http://rdf.disgenet.org/nanopublications.trig#NP680334.RA3kYaeiZMf6vKtXzv0QF_tT88LSz9zoKkc6VYpaCXAVo130_provenance"
}, {
  "@graph" : [ {
    "@id" : "http://rdf.disgenet.org/nanopublications.trig#NP680334.RA3kYaeiZMf6vKtXzv0QF_tT88LSz9zoKkc6VYpaCXAVo",
    "http://purl.org/dc/terms/created" : [ {
      "@type" : "http://www.w3.org/2001/XMLSchema#dateTime",
      "@value" : "2014-10-02T12:38:50+02:00"
    } ],
    "http://purl.org/dc/terms/rights" : [ {
      "@id" : "http://opendatacommons.org/licenses/odbl/1.0/"
    } ],
    "http://purl.org/dc/terms/rightsHolder" : [ {
      "@id" : "http://rdf.disgenet.org/v2.1.0/void.ttl#IBIGroup"
    } ],
    "http://purl.org/dc/terms/subject" : [ {
      "@id" : "http://semanticscience.org/resource/SIO_000983"
    } ],
    "http://purl.org/net/provenance/ns#usedData" : [ {
      "@id" : "http://rdf.disgenet.org/v2.1.0/void.ttl#disgenetrdf"
    } ],
    "http://purl.org/pav/2.0/authoredBy" : [ {
      "@id" : "http://orcid.org/0000-0001-5999-6269"
    }, {
      "@id" : "http://orcid.org/0000-0002-7534-7661"
    }, {
      "@id" : "http://orcid.org/0000-0002-9383-528X"
    }, {
      "@id" : "http://orcid.org/0000-0003-0169-8159"
    }, {
      "@id" : "http://orcid.org/0000-0003-1244-7654"
    } ],
    "http://purl.org/pav/2.0/createdBy" : [ {
      "@id" : "http://orcid.org/0000-0003-0169-8159"
    } ],
    "http://purl.org/pav/2.0/version" : [ {
      "@value" : "v2.1.0.0"
    } ]
  }, {
    "@id" : "http://rdf.disgenet.org/v2.1.0/void.ttl#disgenetrdf",
    "http://purl.org/pav/2.0/version" : [ {
      "@value" : "v2.1.0"
    } ]
  } ],
  "@id" : "http://rdf.disgenet.org/nanopublications.trig#NP680334.RA3kYaeiZMf6vKtXzv0QF_tT88LSz9zoKkc6VYpaCXAVo130_publicationInfo"
} ]