Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP831983.RAVLTPNV6RC5qjlEr_mR5JW2CC0CvaL2CWEl15jiUroNE130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP831983.RAVLTPNV6RC5qjlEr_mR5JW2CC0CvaL2CWEl15jiUroNE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP831983.RAVLTPNV6RC5qjlEr_mR5JW2CC0CvaL2CWEl15jiUroNE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP831983.RAVLTPNV6RC5qjlEr_mR5JW2CC0CvaL2CWEl15jiUroNE130_provenance.
- NP831983.RAVLTPNV6RC5qjlEr_mR5JW2CC0CvaL2CWEl15jiUroNE130_assertion description "[Distinctive genetic and clinical features of CMT4J: a severe neuropathy caused by mutations in the PI(3,5)P? phosphatase FIG4.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP831983.RAVLTPNV6RC5qjlEr_mR5JW2CC0CvaL2CWEl15jiUroNE130_provenance.
- NP831983.RAVLTPNV6RC5qjlEr_mR5JW2CC0CvaL2CWEl15jiUroNE130_assertion evidence source_evidence_literature NP831983.RAVLTPNV6RC5qjlEr_mR5JW2CC0CvaL2CWEl15jiUroNE130_provenance.
- NP831983.RAVLTPNV6RC5qjlEr_mR5JW2CC0CvaL2CWEl15jiUroNE130_assertion SIO_000772 21705420 NP831983.RAVLTPNV6RC5qjlEr_mR5JW2CC0CvaL2CWEl15jiUroNE130_provenance.
- NP831983.RAVLTPNV6RC5qjlEr_mR5JW2CC0CvaL2CWEl15jiUroNE130_assertion wasDerivedFrom befree-20150227 NP831983.RAVLTPNV6RC5qjlEr_mR5JW2CC0CvaL2CWEl15jiUroNE130_provenance.
- NP831983.RAVLTPNV6RC5qjlEr_mR5JW2CC0CvaL2CWEl15jiUroNE130_assertion wasGeneratedBy ECO_0000203 NP831983.RAVLTPNV6RC5qjlEr_mR5JW2CC0CvaL2CWEl15jiUroNE130_provenance.
- befree-20150227 importedOn "2015-02-27" NP831983.RAVLTPNV6RC5qjlEr_mR5JW2CC0CvaL2CWEl15jiUroNE130_provenance.