Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP755206.RAqVA4zHw_yM7Ombfo8TZbvHH5z9vlqyT-BFDZq3Ryfho130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP755206.RAqVA4zHw_yM7Ombfo8TZbvHH5z9vlqyT-BFDZq3Ryfho130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP755206.RAqVA4zHw_yM7Ombfo8TZbvHH5z9vlqyT-BFDZq3Ryfho130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP755206.RAqVA4zHw_yM7Ombfo8TZbvHH5z9vlqyT-BFDZq3Ryfho130_provenance.
- NP755206.RAqVA4zHw_yM7Ombfo8TZbvHH5z9vlqyT-BFDZq3Ryfho130_assertion description "[Two genetic deletions were identified: SPG4delEx17 in 12 of the 13 family members and a deletion of SPG6 (SPG6del) in 5.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP755206.RAqVA4zHw_yM7Ombfo8TZbvHH5z9vlqyT-BFDZq3Ryfho130_provenance.
- NP755206.RAqVA4zHw_yM7Ombfo8TZbvHH5z9vlqyT-BFDZq3Ryfho130_assertion evidence source_evidence_literature NP755206.RAqVA4zHw_yM7Ombfo8TZbvHH5z9vlqyT-BFDZq3Ryfho130_provenance.
- NP755206.RAqVA4zHw_yM7Ombfo8TZbvHH5z9vlqyT-BFDZq3Ryfho130_assertion SIO_000772 19652142 NP755206.RAqVA4zHw_yM7Ombfo8TZbvHH5z9vlqyT-BFDZq3Ryfho130_provenance.
- NP755206.RAqVA4zHw_yM7Ombfo8TZbvHH5z9vlqyT-BFDZq3Ryfho130_assertion wasDerivedFrom befree-2016 NP755206.RAqVA4zHw_yM7Ombfo8TZbvHH5z9vlqyT-BFDZq3Ryfho130_provenance.
- NP755206.RAqVA4zHw_yM7Ombfo8TZbvHH5z9vlqyT-BFDZq3Ryfho130_assertion wasGeneratedBy ECO_0000203 NP755206.RAqVA4zHw_yM7Ombfo8TZbvHH5z9vlqyT-BFDZq3Ryfho130_provenance.
- befree-2016 importedOn "2016-02-19" NP755206.RAqVA4zHw_yM7Ombfo8TZbvHH5z9vlqyT-BFDZq3Ryfho130_provenance.