Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP153815.RA6Qt54cLQD2yctKDQsOD1SqnsvyQdhpW4Dmy39NNgHC4130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP153815.RA6Qt54cLQD2yctKDQsOD1SqnsvyQdhpW4Dmy39NNgHC4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP153815.RA6Qt54cLQD2yctKDQsOD1SqnsvyQdhpW4Dmy39NNgHC4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP153815.RA6Qt54cLQD2yctKDQsOD1SqnsvyQdhpW4Dmy39NNgHC4130_provenance.
- NP153815.RA6Qt54cLQD2yctKDQsOD1SqnsvyQdhpW4Dmy39NNgHC4130_assertion description "[Loss of ESCO2 acetyltransferase activity contributes to the pathogenesis of Roberts syndrome/SC phocomelia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP153815.RA6Qt54cLQD2yctKDQsOD1SqnsvyQdhpW4Dmy39NNgHC4130_provenance.
- NP153815.RA6Qt54cLQD2yctKDQsOD1SqnsvyQdhpW4Dmy39NNgHC4130_assertion evidence source_evidence_literature NP153815.RA6Qt54cLQD2yctKDQsOD1SqnsvyQdhpW4Dmy39NNgHC4130_provenance.
- NP153815.RA6Qt54cLQD2yctKDQsOD1SqnsvyQdhpW4Dmy39NNgHC4130_assertion SIO_000772 18411254 NP153815.RA6Qt54cLQD2yctKDQsOD1SqnsvyQdhpW4Dmy39NNgHC4130_provenance.
- NP153815.RA6Qt54cLQD2yctKDQsOD1SqnsvyQdhpW4Dmy39NNgHC4130_assertion wasDerivedFrom lhgdn-20090331 NP153815.RA6Qt54cLQD2yctKDQsOD1SqnsvyQdhpW4Dmy39NNgHC4130_provenance.
- NP153815.RA6Qt54cLQD2yctKDQsOD1SqnsvyQdhpW4Dmy39NNgHC4130_assertion wasGeneratedBy ECO_0000203 NP153815.RA6Qt54cLQD2yctKDQsOD1SqnsvyQdhpW4Dmy39NNgHC4130_provenance.
- lhgdn-20090331 importedOn "2009-03-31" NP153815.RA6Qt54cLQD2yctKDQsOD1SqnsvyQdhpW4Dmy39NNgHC4130_provenance.