@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP271741.RAKKmjfeUhBg3qb_AtdU8VZMU6f0x3V4fFQAL8UBodrHs> .
@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:NP271741.RAKKmjfeUhBg3qb_AtdU8VZMU6f0x3V4fFQAL8UBodrHs130_head {
  this: np:hasAssertion dgn-np:NP271741.RAKKmjfeUhBg3qb_AtdU8VZMU6f0x3V4fFQAL8UBodrHs130_assertion ;
    np:hasProvenance dgn-np:NP271741.RAKKmjfeUhBg3qb_AtdU8VZMU6f0x3V4fFQAL8UBodrHs130_provenance ;
    np:hasPublicationInfo dgn-np:NP271741.RAKKmjfeUhBg3qb_AtdU8VZMU6f0x3V4fFQAL8UBodrHs130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP271741.RAKKmjfeUhBg3qb_AtdU8VZMU6f0x3V4fFQAL8UBodrHs130_assertion a np:Assertion .
  dgn-np:NP271741.RAKKmjfeUhBg3qb_AtdU8VZMU6f0x3V4fFQAL8UBodrHs130_provenance a np:Provenance .
  dgn-np:NP271741.RAKKmjfeUhBg3qb_AtdU8VZMU6f0x3V4fFQAL8UBodrHs130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP271741.RAKKmjfeUhBg3qb_AtdU8VZMU6f0x3V4fFQAL8UBodrHs130_assertion {
  miriam-gene:6559 a ncit:C16612 .
  lld:C0085580 a ncit:C7057 .
  dgn-gda:DGN1c722411270dec526afe56e111f5e4ff sio:SIO_000628 miriam-gene:6559 , lld:C0085580 ;
    a sio:SIO_001121 .
}
dgn-np:NP271741.RAKKmjfeUhBg3qb_AtdU8VZMU6f0x3V4fFQAL8UBodrHs130_provenance {
  dgn-np:NP271741.RAKKmjfeUhBg3qb_AtdU8VZMU6f0x3V4fFQAL8UBodrHs130_assertion dcterms:description "[Our results show that the substitution of arginine for cysteine at position 919 of TSC increases Na transport function, and provide support for the hypothesis that mutations in renal tubular sodium transporters may contribute to the development of primary hypertension, a polygenic disorder, by increasing renal sodium reabsorption.]. 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:17885550 ;
    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:NP271741.RAKKmjfeUhBg3qb_AtdU8VZMU6f0x3V4fFQAL8UBodrHs130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:33+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" .
}