Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP598510.RANlI35NY9oxivJQR5t3qPlPPu_2w-csdMIpVypNwAZEQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP598510.RANlI35NY9oxivJQR5t3qPlPPu_2w-csdMIpVypNwAZEQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP598510.RANlI35NY9oxivJQR5t3qPlPPu_2w-csdMIpVypNwAZEQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP598510.RANlI35NY9oxivJQR5t3qPlPPu_2w-csdMIpVypNwAZEQ130_provenance.
- NP598510.RANlI35NY9oxivJQR5t3qPlPPu_2w-csdMIpVypNwAZEQ130_assertion description "[To investigate the presence of mutations in the parkin gene and the A265G variant in the HS1BP3 gene in a Mexican family with EOPD, ET, and Bell palsy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP598510.RANlI35NY9oxivJQR5t3qPlPPu_2w-csdMIpVypNwAZEQ130_provenance.
- NP598510.RANlI35NY9oxivJQR5t3qPlPPu_2w-csdMIpVypNwAZEQ130_assertion evidence source_evidence_literature NP598510.RANlI35NY9oxivJQR5t3qPlPPu_2w-csdMIpVypNwAZEQ130_provenance.
- NP598510.RANlI35NY9oxivJQR5t3qPlPPu_2w-csdMIpVypNwAZEQ130_assertion SIO_000772 17353387 NP598510.RANlI35NY9oxivJQR5t3qPlPPu_2w-csdMIpVypNwAZEQ130_provenance.
- NP598510.RANlI35NY9oxivJQR5t3qPlPPu_2w-csdMIpVypNwAZEQ130_assertion wasDerivedFrom befree-2016 NP598510.RANlI35NY9oxivJQR5t3qPlPPu_2w-csdMIpVypNwAZEQ130_provenance.
- NP598510.RANlI35NY9oxivJQR5t3qPlPPu_2w-csdMIpVypNwAZEQ130_assertion wasGeneratedBy ECO_0000203 NP598510.RANlI35NY9oxivJQR5t3qPlPPu_2w-csdMIpVypNwAZEQ130_provenance.
- befree-2016 importedOn "2016-02-19" NP598510.RANlI35NY9oxivJQR5t3qPlPPu_2w-csdMIpVypNwAZEQ130_provenance.