Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1232251.RAPGOcPHSZZ09O_ZMBjWYg0LAPWsUZUUNgq4EXjdfQX-k130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1232251.RAPGOcPHSZZ09O_ZMBjWYg0LAPWsUZUUNgq4EXjdfQX-k130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1232251.RAPGOcPHSZZ09O_ZMBjWYg0LAPWsUZUUNgq4EXjdfQX-k130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1232251.RAPGOcPHSZZ09O_ZMBjWYg0LAPWsUZUUNgq4EXjdfQX-k130_provenance.
- NP1232251.RAPGOcPHSZZ09O_ZMBjWYg0LAPWsUZUUNgq4EXjdfQX-k130_assertion description "[Mutations in the HINT1 gene were recently discovered as being the major cause of autosomal recessive axonal neuropathy with neuromyotonia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1232251.RAPGOcPHSZZ09O_ZMBjWYg0LAPWsUZUUNgq4EXjdfQX-k130_provenance.
- NP1232251.RAPGOcPHSZZ09O_ZMBjWYg0LAPWsUZUUNgq4EXjdfQX-k130_assertion evidence source_evidence_literature NP1232251.RAPGOcPHSZZ09O_ZMBjWYg0LAPWsUZUUNgq4EXjdfQX-k130_provenance.
- NP1232251.RAPGOcPHSZZ09O_ZMBjWYg0LAPWsUZUUNgq4EXjdfQX-k130_assertion SIO_000772 25342199 NP1232251.RAPGOcPHSZZ09O_ZMBjWYg0LAPWsUZUUNgq4EXjdfQX-k130_provenance.
- NP1232251.RAPGOcPHSZZ09O_ZMBjWYg0LAPWsUZUUNgq4EXjdfQX-k130_assertion wasDerivedFrom befree-2016 NP1232251.RAPGOcPHSZZ09O_ZMBjWYg0LAPWsUZUUNgq4EXjdfQX-k130_provenance.
- NP1232251.RAPGOcPHSZZ09O_ZMBjWYg0LAPWsUZUUNgq4EXjdfQX-k130_assertion wasGeneratedBy ECO_0000203 NP1232251.RAPGOcPHSZZ09O_ZMBjWYg0LAPWsUZUUNgq4EXjdfQX-k130_provenance.
- befree-2016 importedOn "2016-02-19" NP1232251.RAPGOcPHSZZ09O_ZMBjWYg0LAPWsUZUUNgq4EXjdfQX-k130_provenance.