@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP545562.RAShJuZ1ii6k_qRf7fP_EskaYDG4Em2wwtiFZzACeOxKI> .
@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:NP545562.RAShJuZ1ii6k_qRf7fP_EskaYDG4Em2wwtiFZzACeOxKI130_head {
  this: np:hasAssertion dgn-np:NP545562.RAShJuZ1ii6k_qRf7fP_EskaYDG4Em2wwtiFZzACeOxKI130_assertion;
    np:hasProvenance dgn-np:NP545562.RAShJuZ1ii6k_qRf7fP_EskaYDG4Em2wwtiFZzACeOxKI130_provenance;
    np:hasPublicationInfo dgn-np:NP545562.RAShJuZ1ii6k_qRf7fP_EskaYDG4Em2wwtiFZzACeOxKI130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP545562.RAShJuZ1ii6k_qRf7fP_EskaYDG4Em2wwtiFZzACeOxKI130_assertion a np:Assertion .
  
  dgn-np:NP545562.RAShJuZ1ii6k_qRf7fP_EskaYDG4Em2wwtiFZzACeOxKI130_provenance a np:Provenance .
  
  dgn-np:NP545562.RAShJuZ1ii6k_qRf7fP_EskaYDG4Em2wwtiFZzACeOxKI130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP545562.RAShJuZ1ii6k_qRf7fP_EskaYDG4Em2wwtiFZzACeOxKI130_assertion {
  miriam-gene:7170 a ncit:C16612 .
  
  lld:C0035334 a ncit:C7057 .
  
  dgn-gda:DGNd63772d6b5ff60dd08b762316fc00ea3 sio:SIO_000628 miriam-gene:7170, lld:C0035334;
    a sio:SIO_001121 .
}

dgn-np:NP545562.RAShJuZ1ii6k_qRf7fP_EskaYDG4Em2wwtiFZzACeOxKI130_provenance {
  dgn-np:NP545562.RAShJuZ1ii6k_qRf7fP_EskaYDG4Em2wwtiFZzACeOxKI130_assertion dcterms:description
      "[Further, analysis of another retinitis pigmentosa mutation, A164V (TM IV), indicates that the larger Val interferes with residues Leu119 and Ile123 on TM III, leading to the disruption of the same critical Glu122-His211 salt bridge (TM III-TM V interaction).]. 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:12871954;
    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:NP545562.RAShJuZ1ii6k_qRf7fP_EskaYDG4Em2wwtiFZzACeOxKI130_publicationInfo {
  this: dcterms:created "2014-10-02T12:37:29+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" .
}