Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1344276.RA78HB7evMSaEVwwalV0TVzmh9mCQkcwh8742DZQxCjV4130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1344276.RA78HB7evMSaEVwwalV0TVzmh9mCQkcwh8742DZQxCjV4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1344276.RA78HB7evMSaEVwwalV0TVzmh9mCQkcwh8742DZQxCjV4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1344276.RA78HB7evMSaEVwwalV0TVzmh9mCQkcwh8742DZQxCjV4130_provenance.
- NP1344276.RA78HB7evMSaEVwwalV0TVzmh9mCQkcwh8742DZQxCjV4130_assertion description "[The cloning of FALDH and the identification of mutations in SLS patients opens up possibilities for developing therapeutic approaches to ameliorate the neurologic and cutaneous symptoms of the disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1344276.RA78HB7evMSaEVwwalV0TVzmh9mCQkcwh8742DZQxCjV4130_provenance.
- NP1344276.RA78HB7evMSaEVwwalV0TVzmh9mCQkcwh8742DZQxCjV4130_assertion evidence source_evidence_literature NP1344276.RA78HB7evMSaEVwwalV0TVzmh9mCQkcwh8742DZQxCjV4130_provenance.
- NP1344276.RA78HB7evMSaEVwwalV0TVzmh9mCQkcwh8742DZQxCjV4130_assertion SIO_000772 8528251 NP1344276.RA78HB7evMSaEVwwalV0TVzmh9mCQkcwh8742DZQxCjV4130_provenance.
- NP1344276.RA78HB7evMSaEVwwalV0TVzmh9mCQkcwh8742DZQxCjV4130_assertion wasDerivedFrom befree-2016 NP1344276.RA78HB7evMSaEVwwalV0TVzmh9mCQkcwh8742DZQxCjV4130_provenance.
- NP1344276.RA78HB7evMSaEVwwalV0TVzmh9mCQkcwh8742DZQxCjV4130_assertion wasGeneratedBy ECO_0000203 NP1344276.RA78HB7evMSaEVwwalV0TVzmh9mCQkcwh8742DZQxCjV4130_provenance.
- befree-2016 importedOn "2016-02-19" NP1344276.RA78HB7evMSaEVwwalV0TVzmh9mCQkcwh8742DZQxCjV4130_provenance.