Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP948331.RAPwX7w60o9_RUxtulj5pHnuTPHSqPIdDAVC_EKz2aSFo130_assertion> ?p ?o ?g. }
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- NP948331.RAPwX7w60o9_RUxtulj5pHnuTPHSqPIdDAVC_EKz2aSFo130_assertion type Assertion NP948331.RAPwX7w60o9_RUxtulj5pHnuTPHSqPIdDAVC_EKz2aSFo130_head.
- NP948331.RAPwX7w60o9_RUxtulj5pHnuTPHSqPIdDAVC_EKz2aSFo130_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." NP948331.RAPwX7w60o9_RUxtulj5pHnuTPHSqPIdDAVC_EKz2aSFo130_provenance.
- NP948331.RAPwX7w60o9_RUxtulj5pHnuTPHSqPIdDAVC_EKz2aSFo130_assertion evidence source_evidence_literature NP948331.RAPwX7w60o9_RUxtulj5pHnuTPHSqPIdDAVC_EKz2aSFo130_provenance.
- NP948331.RAPwX7w60o9_RUxtulj5pHnuTPHSqPIdDAVC_EKz2aSFo130_assertion SIO_000772 22187434 NP948331.RAPwX7w60o9_RUxtulj5pHnuTPHSqPIdDAVC_EKz2aSFo130_provenance.
- NP948331.RAPwX7w60o9_RUxtulj5pHnuTPHSqPIdDAVC_EKz2aSFo130_assertion wasDerivedFrom befree-2016 NP948331.RAPwX7w60o9_RUxtulj5pHnuTPHSqPIdDAVC_EKz2aSFo130_provenance.
- NP948331.RAPwX7w60o9_RUxtulj5pHnuTPHSqPIdDAVC_EKz2aSFo130_assertion wasGeneratedBy ECO_0000203 NP948331.RAPwX7w60o9_RUxtulj5pHnuTPHSqPIdDAVC_EKz2aSFo130_provenance.