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- NP935171.RAJe28oZGHEcww-6m61TbmwX-YObx5wqGy5whqTlslJqE130_assertion type Assertion NP935171.RAJe28oZGHEcww-6m61TbmwX-YObx5wqGy5whqTlslJqE130_head.
- NP935171.RAJe28oZGHEcww-6m61TbmwX-YObx5wqGy5whqTlslJqE130_assertion description "[Recent advances in genetics have resulted in the identification of missense mutations in TRPV4 in patients with these hereditary neuropathies.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP935171.RAJe28oZGHEcww-6m61TbmwX-YObx5wqGy5whqTlslJqE130_provenance.
- NP935171.RAJe28oZGHEcww-6m61TbmwX-YObx5wqGy5whqTlslJqE130_assertion evidence source_evidence_literature NP935171.RAJe28oZGHEcww-6m61TbmwX-YObx5wqGy5whqTlslJqE130_provenance.
- NP935171.RAJe28oZGHEcww-6m61TbmwX-YObx5wqGy5whqTlslJqE130_assertion SIO_000772 22187434 NP935171.RAJe28oZGHEcww-6m61TbmwX-YObx5wqGy5whqTlslJqE130_provenance.
- NP935171.RAJe28oZGHEcww-6m61TbmwX-YObx5wqGy5whqTlslJqE130_assertion wasDerivedFrom befree-20150227 NP935171.RAJe28oZGHEcww-6m61TbmwX-YObx5wqGy5whqTlslJqE130_provenance.
- NP935171.RAJe28oZGHEcww-6m61TbmwX-YObx5wqGy5whqTlslJqE130_assertion wasGeneratedBy ECO_0000203 NP935171.RAJe28oZGHEcww-6m61TbmwX-YObx5wqGy5whqTlslJqE130_provenance.