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- source_evidence_literature type ECO_0000212 NP1011411.RA41lJ5BKhckjaMcErI4J5Ckxtk0UVW9-twyPJAUO1Eqw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1011411.RA41lJ5BKhckjaMcErI4J5Ckxtk0UVW9-twyPJAUO1Eqw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1011411.RA41lJ5BKhckjaMcErI4J5Ckxtk0UVW9-twyPJAUO1Eqw130_provenance.
- befree-2016 importedOn "2016-02-19" NP1011411.RA41lJ5BKhckjaMcErI4J5Ckxtk0UVW9-twyPJAUO1Eqw130_provenance.
- NP1011411.RA41lJ5BKhckjaMcErI4J5Ckxtk0UVW9-twyPJAUO1Eqw130_assertion wasGeneratedBy ECO_0000203 NP1011411.RA41lJ5BKhckjaMcErI4J5Ckxtk0UVW9-twyPJAUO1Eqw130_provenance.
- NP1011411.RA41lJ5BKhckjaMcErI4J5Ckxtk0UVW9-twyPJAUO1Eqw130_assertion wasDerivedFrom befree-2016 NP1011411.RA41lJ5BKhckjaMcErI4J5Ckxtk0UVW9-twyPJAUO1Eqw130_provenance.
- NP1011411.RA41lJ5BKhckjaMcErI4J5Ckxtk0UVW9-twyPJAUO1Eqw130_assertion SIO_000772 22961002 NP1011411.RA41lJ5BKhckjaMcErI4J5Ckxtk0UVW9-twyPJAUO1Eqw130_provenance.
- NP1011411.RA41lJ5BKhckjaMcErI4J5Ckxtk0UVW9-twyPJAUO1Eqw130_assertion evidence source_evidence_literature NP1011411.RA41lJ5BKhckjaMcErI4J5Ckxtk0UVW9-twyPJAUO1Eqw130_provenance.
- NP1011411.RA41lJ5BKhckjaMcErI4J5Ckxtk0UVW9-twyPJAUO1Eqw130_assertion description "[Loss-of-function mutations in HINT1 cause axonal neuropathy with neuromyotonia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1011411.RA41lJ5BKhckjaMcErI4J5Ckxtk0UVW9-twyPJAUO1Eqw130_provenance.