Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP606584.RASFIlw2kOEb3tQ3eCF5VrtDshjNYVWQBHyVP6LZIZ36Q130_assertion> ?p ?o ?g. }
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- NP606584.RASFIlw2kOEb3tQ3eCF5VrtDshjNYVWQBHyVP6LZIZ36Q130_assertion type Assertion NP606584.RASFIlw2kOEb3tQ3eCF5VrtDshjNYVWQBHyVP6LZIZ36Q130_head.
- NP606584.RASFIlw2kOEb3tQ3eCF5VrtDshjNYVWQBHyVP6LZIZ36Q130_assertion description "[We identified pathogenic mutations of human FIG4 (KIAA0274) on chromosome 6q21 in four unrelated patients with hereditary motor and sensory neuropathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP606584.RASFIlw2kOEb3tQ3eCF5VrtDshjNYVWQBHyVP6LZIZ36Q130_provenance.
- NP606584.RASFIlw2kOEb3tQ3eCF5VrtDshjNYVWQBHyVP6LZIZ36Q130_assertion evidence source_evidence_literature NP606584.RASFIlw2kOEb3tQ3eCF5VrtDshjNYVWQBHyVP6LZIZ36Q130_provenance.
- NP606584.RASFIlw2kOEb3tQ3eCF5VrtDshjNYVWQBHyVP6LZIZ36Q130_assertion SIO_000772 17572665 NP606584.RASFIlw2kOEb3tQ3eCF5VrtDshjNYVWQBHyVP6LZIZ36Q130_provenance.
- NP606584.RASFIlw2kOEb3tQ3eCF5VrtDshjNYVWQBHyVP6LZIZ36Q130_assertion wasDerivedFrom befree-20140225 NP606584.RASFIlw2kOEb3tQ3eCF5VrtDshjNYVWQBHyVP6LZIZ36Q130_provenance.
- NP606584.RASFIlw2kOEb3tQ3eCF5VrtDshjNYVWQBHyVP6LZIZ36Q130_assertion wasGeneratedBy ECO_0000203 NP606584.RASFIlw2kOEb3tQ3eCF5VrtDshjNYVWQBHyVP6LZIZ36Q130_provenance.