Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP926983.RABJhnGq02v3faMRYEEDECI3FrlHia4MHbS2gRQ2enaHE130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP926983.RABJhnGq02v3faMRYEEDECI3FrlHia4MHbS2gRQ2enaHE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP926983.RABJhnGq02v3faMRYEEDECI3FrlHia4MHbS2gRQ2enaHE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP926983.RABJhnGq02v3faMRYEEDECI3FrlHia4MHbS2gRQ2enaHE130_provenance.
- NP926983.RABJhnGq02v3faMRYEEDECI3FrlHia4MHbS2gRQ2enaHE130_assertion description "[Here, we report for the first time that mutations in CABP4 lead to autosomal recessive CSNB.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP926983.RABJhnGq02v3faMRYEEDECI3FrlHia4MHbS2gRQ2enaHE130_provenance.
- NP926983.RABJhnGq02v3faMRYEEDECI3FrlHia4MHbS2gRQ2enaHE130_assertion evidence source_evidence_literature NP926983.RABJhnGq02v3faMRYEEDECI3FrlHia4MHbS2gRQ2enaHE130_provenance.
- NP926983.RABJhnGq02v3faMRYEEDECI3FrlHia4MHbS2gRQ2enaHE130_assertion SIO_000772 16960802 NP926983.RABJhnGq02v3faMRYEEDECI3FrlHia4MHbS2gRQ2enaHE130_provenance.
- NP926983.RABJhnGq02v3faMRYEEDECI3FrlHia4MHbS2gRQ2enaHE130_assertion wasDerivedFrom befree-20150227 NP926983.RABJhnGq02v3faMRYEEDECI3FrlHia4MHbS2gRQ2enaHE130_provenance.
- NP926983.RABJhnGq02v3faMRYEEDECI3FrlHia4MHbS2gRQ2enaHE130_assertion wasGeneratedBy ECO_0000203 NP926983.RABJhnGq02v3faMRYEEDECI3FrlHia4MHbS2gRQ2enaHE130_provenance.
- befree-20150227 importedOn "2015-02-27" NP926983.RABJhnGq02v3faMRYEEDECI3FrlHia4MHbS2gRQ2enaHE130_provenance.