Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP780924.RAPBDeDFnqUIdrDiCvjxe3tPJJwmBF__g4GMfg9GFcSZI130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP780924.RAPBDeDFnqUIdrDiCvjxe3tPJJwmBF__g4GMfg9GFcSZI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP780924.RAPBDeDFnqUIdrDiCvjxe3tPJJwmBF__g4GMfg9GFcSZI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP780924.RAPBDeDFnqUIdrDiCvjxe3tPJJwmBF__g4GMfg9GFcSZI130_provenance.
- NP780924.RAPBDeDFnqUIdrDiCvjxe3tPJJwmBF__g4GMfg9GFcSZI130_assertion description "[Expanding the phenotypes of the Pro56Ser VAPB mutation: proximal SMA with dysautonomia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP780924.RAPBDeDFnqUIdrDiCvjxe3tPJJwmBF__g4GMfg9GFcSZI130_provenance.
- NP780924.RAPBDeDFnqUIdrDiCvjxe3tPJJwmBF__g4GMfg9GFcSZI130_assertion evidence source_evidence_literature NP780924.RAPBDeDFnqUIdrDiCvjxe3tPJJwmBF__g4GMfg9GFcSZI130_provenance.
- NP780924.RAPBDeDFnqUIdrDiCvjxe3tPJJwmBF__g4GMfg9GFcSZI130_assertion SIO_000772 16967488 NP780924.RAPBDeDFnqUIdrDiCvjxe3tPJJwmBF__g4GMfg9GFcSZI130_provenance.
- NP780924.RAPBDeDFnqUIdrDiCvjxe3tPJJwmBF__g4GMfg9GFcSZI130_assertion wasDerivedFrom befree-20140225 NP780924.RAPBDeDFnqUIdrDiCvjxe3tPJJwmBF__g4GMfg9GFcSZI130_provenance.
- NP780924.RAPBDeDFnqUIdrDiCvjxe3tPJJwmBF__g4GMfg9GFcSZI130_assertion wasGeneratedBy ECO_0000203 NP780924.RAPBDeDFnqUIdrDiCvjxe3tPJJwmBF__g4GMfg9GFcSZI130_provenance.
- befree-20140225 importedOn "2014-02-25" NP780924.RAPBDeDFnqUIdrDiCvjxe3tPJJwmBF__g4GMfg9GFcSZI130_provenance.