Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP618444.RAjdVDhzFXlJOfMKPLWVnFutCH4RiDK4g4JpNqaSrqFbo130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP618444.RAjdVDhzFXlJOfMKPLWVnFutCH4RiDK4g4JpNqaSrqFbo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP618444.RAjdVDhzFXlJOfMKPLWVnFutCH4RiDK4g4JpNqaSrqFbo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP618444.RAjdVDhzFXlJOfMKPLWVnFutCH4RiDK4g4JpNqaSrqFbo130_provenance.
- NP618444.RAjdVDhzFXlJOfMKPLWVnFutCH4RiDK4g4JpNqaSrqFbo130_assertion description "[However, some of the mutants still possess autolytic activity and/or connectin/titin binding ability, indicating these properties are not necessary for the LGMD2A phenotypes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP618444.RAjdVDhzFXlJOfMKPLWVnFutCH4RiDK4g4JpNqaSrqFbo130_provenance.
- NP618444.RAjdVDhzFXlJOfMKPLWVnFutCH4RiDK4g4JpNqaSrqFbo130_assertion evidence source_evidence_literature NP618444.RAjdVDhzFXlJOfMKPLWVnFutCH4RiDK4g4JpNqaSrqFbo130_provenance.
- NP618444.RAjdVDhzFXlJOfMKPLWVnFutCH4RiDK4g4JpNqaSrqFbo130_assertion SIO_000772 9642272 NP618444.RAjdVDhzFXlJOfMKPLWVnFutCH4RiDK4g4JpNqaSrqFbo130_provenance.
- NP618444.RAjdVDhzFXlJOfMKPLWVnFutCH4RiDK4g4JpNqaSrqFbo130_assertion wasDerivedFrom befree-20140225 NP618444.RAjdVDhzFXlJOfMKPLWVnFutCH4RiDK4g4JpNqaSrqFbo130_provenance.
- NP618444.RAjdVDhzFXlJOfMKPLWVnFutCH4RiDK4g4JpNqaSrqFbo130_assertion wasGeneratedBy ECO_0000203 NP618444.RAjdVDhzFXlJOfMKPLWVnFutCH4RiDK4g4JpNqaSrqFbo130_provenance.
- befree-20140225 importedOn "2014-02-25" NP618444.RAjdVDhzFXlJOfMKPLWVnFutCH4RiDK4g4JpNqaSrqFbo130_provenance.