@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP944981.RAnt1N9-ahW0SBydnT9B__zDIQ3oG1dY-aLiXEgJgWy-I> .
@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/> .
@prefix wi: <http://purl.org/ontology/wi/core#> .
@prefix prov: <http://www.w3.org/ns/prov#> .
@prefix pav: <http://purl.org/pav/> .
@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/resource/nanopub/> .
@prefix dgn-gda: <http://rdf.disgenet.org/resource/gda/> .
@prefix dgn-void: <http://rdf.disgenet.org/v3.0.0/void/> .
dgn-np:NP944981.RAnt1N9-ahW0SBydnT9B__zDIQ3oG1dY-aLiXEgJgWy-I130_head {
  this: np:hasAssertion dgn-np:NP944981.RAnt1N9-ahW0SBydnT9B__zDIQ3oG1dY-aLiXEgJgWy-I130_assertion ;
    np:hasProvenance dgn-np:NP944981.RAnt1N9-ahW0SBydnT9B__zDIQ3oG1dY-aLiXEgJgWy-I130_provenance ;
    np:hasPublicationInfo dgn-np:NP944981.RAnt1N9-ahW0SBydnT9B__zDIQ3oG1dY-aLiXEgJgWy-I130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP944981.RAnt1N9-ahW0SBydnT9B__zDIQ3oG1dY-aLiXEgJgWy-I130_assertion a np:Assertion .
  dgn-np:NP944981.RAnt1N9-ahW0SBydnT9B__zDIQ3oG1dY-aLiXEgJgWy-I130_provenance a np:Provenance .
  dgn-np:NP944981.RAnt1N9-ahW0SBydnT9B__zDIQ3oG1dY-aLiXEgJgWy-I130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP944981.RAnt1N9-ahW0SBydnT9B__zDIQ3oG1dY-aLiXEgJgWy-I130_assertion {
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}
dgn-np:NP944981.RAnt1N9-ahW0SBydnT9B__zDIQ3oG1dY-aLiXEgJgWy-I130_provenance {
  dgn-np:NP944981.RAnt1N9-ahW0SBydnT9B__zDIQ3oG1dY-aLiXEgJgWy-I130_assertion dcterms:description "[We apply s-RT-MELT in the screening of p53 and EGFR mutations in cell lines and clinical samples and demonstrate its advantages for rapid, multiplexed mutation scanning in cancer and for genetic variation screening in biology and medicine.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ;
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    sio:SIO_000772 miriam-pubmed:17545195 ;
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  dgn-void:source_evidence_literature a eco:ECO_0000212 ;
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}
dgn-np:NP944981.RAnt1N9-ahW0SBydnT9B__zDIQ3oG1dY-aLiXEgJgWy-I130_publicationInfo {
  this: dcterms:created "2015-08-25T14:47:17+02:00"^^xsd:dateTime ;
    dcterms:rights <http://opendatacommons.org/licenses/odbl/1.0/> ;
    dcterms:rightsHolder dgn-void:IBIGroup ;
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}