Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1232260.RAs1gcU8y8Y4IL_M3Sj4UWtVVVUJmfSux918qdWyaw-D0130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1232260.RAs1gcU8y8Y4IL_M3Sj4UWtVVVUJmfSux918qdWyaw-D0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1232260.RAs1gcU8y8Y4IL_M3Sj4UWtVVVUJmfSux918qdWyaw-D0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1232260.RAs1gcU8y8Y4IL_M3Sj4UWtVVVUJmfSux918qdWyaw-D0130_provenance.
- NP1232260.RAs1gcU8y8Y4IL_M3Sj4UWtVVVUJmfSux918qdWyaw-D0130_assertion description "[Mutations in HINT1 are one of the most frequent causes of hereditary neuropathy among Czech patients and neuromyotonia is rather an underdiagnosed symptom.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1232260.RAs1gcU8y8Y4IL_M3Sj4UWtVVVUJmfSux918qdWyaw-D0130_provenance.
- NP1232260.RAs1gcU8y8Y4IL_M3Sj4UWtVVVUJmfSux918qdWyaw-D0130_assertion evidence source_evidence_literature NP1232260.RAs1gcU8y8Y4IL_M3Sj4UWtVVVUJmfSux918qdWyaw-D0130_provenance.
- NP1232260.RAs1gcU8y8Y4IL_M3Sj4UWtVVVUJmfSux918qdWyaw-D0130_assertion SIO_000772 25342199 NP1232260.RAs1gcU8y8Y4IL_M3Sj4UWtVVVUJmfSux918qdWyaw-D0130_provenance.
- NP1232260.RAs1gcU8y8Y4IL_M3Sj4UWtVVVUJmfSux918qdWyaw-D0130_assertion wasDerivedFrom befree-2016 NP1232260.RAs1gcU8y8Y4IL_M3Sj4UWtVVVUJmfSux918qdWyaw-D0130_provenance.
- NP1232260.RAs1gcU8y8Y4IL_M3Sj4UWtVVVUJmfSux918qdWyaw-D0130_assertion wasGeneratedBy ECO_0000203 NP1232260.RAs1gcU8y8Y4IL_M3Sj4UWtVVVUJmfSux918qdWyaw-D0130_provenance.
- befree-2016 importedOn "2016-02-19" NP1232260.RAs1gcU8y8Y4IL_M3Sj4UWtVVVUJmfSux918qdWyaw-D0130_provenance.