Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP515286.RAcj977X6qev-T9qw-5Mko90-eip00rAhbcBTs8lnC6eU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP515286.RAcj977X6qev-T9qw-5Mko90-eip00rAhbcBTs8lnC6eU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP515286.RAcj977X6qev-T9qw-5Mko90-eip00rAhbcBTs8lnC6eU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP515286.RAcj977X6qev-T9qw-5Mko90-eip00rAhbcBTs8lnC6eU130_provenance.
- NP515286.RAcj977X6qev-T9qw-5Mko90-eip00rAhbcBTs8lnC6eU130_assertion description "[The deficient activity of the human lysosomal hydrolase, acid sphingomyelinase (ASM, EC 3.1.4.12), results in the neuronopathic (Type A) and non-neuronopathic (Type B) forms of Niemann-Pick disease (NPD).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP515286.RAcj977X6qev-T9qw-5Mko90-eip00rAhbcBTs8lnC6eU130_provenance.
- NP515286.RAcj977X6qev-T9qw-5Mko90-eip00rAhbcBTs8lnC6eU130_assertion evidence source_evidence_literature NP515286.RAcj977X6qev-T9qw-5Mko90-eip00rAhbcBTs8lnC6eU130_provenance.
- NP515286.RAcj977X6qev-T9qw-5Mko90-eip00rAhbcBTs8lnC6eU130_assertion SIO_000772 1618760 NP515286.RAcj977X6qev-T9qw-5Mko90-eip00rAhbcBTs8lnC6eU130_provenance.
- NP515286.RAcj977X6qev-T9qw-5Mko90-eip00rAhbcBTs8lnC6eU130_assertion wasDerivedFrom befree-2016 NP515286.RAcj977X6qev-T9qw-5Mko90-eip00rAhbcBTs8lnC6eU130_provenance.
- NP515286.RAcj977X6qev-T9qw-5Mko90-eip00rAhbcBTs8lnC6eU130_assertion wasGeneratedBy ECO_0000203 NP515286.RAcj977X6qev-T9qw-5Mko90-eip00rAhbcBTs8lnC6eU130_provenance.
- befree-2016 importedOn "2016-02-19" NP515286.RAcj977X6qev-T9qw-5Mko90-eip00rAhbcBTs8lnC6eU130_provenance.