Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP826682.RABIbbH78Okw9tItxlcAlfEqcj7U5Lc9cJ2RGOse9a9IU130_assertion> ?p ?o ?g. }
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- NP826682.RABIbbH78Okw9tItxlcAlfEqcj7U5Lc9cJ2RGOse9a9IU130_assertion type Assertion NP826682.RABIbbH78Okw9tItxlcAlfEqcj7U5Lc9cJ2RGOse9a9IU130_head.
- NP826682.RABIbbH78Okw9tItxlcAlfEqcj7U5Lc9cJ2RGOse9a9IU130_assertion description "[Adding to the clinical and molecular heterogeneity of TRPV4-associated diseases, our results suggest that molecular testing of the TRPV4 gene is warranted in cases of congenital dSMA with bone abnormalities and vocal cord paralysis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP826682.RABIbbH78Okw9tItxlcAlfEqcj7U5Lc9cJ2RGOse9a9IU130_provenance.
- NP826682.RABIbbH78Okw9tItxlcAlfEqcj7U5Lc9cJ2RGOse9a9IU130_assertion evidence source_evidence_literature NP826682.RABIbbH78Okw9tItxlcAlfEqcj7U5Lc9cJ2RGOse9a9IU130_provenance.
- NP826682.RABIbbH78Okw9tItxlcAlfEqcj7U5Lc9cJ2RGOse9a9IU130_assertion SIO_000772 22526352 NP826682.RABIbbH78Okw9tItxlcAlfEqcj7U5Lc9cJ2RGOse9a9IU130_provenance.
- NP826682.RABIbbH78Okw9tItxlcAlfEqcj7U5Lc9cJ2RGOse9a9IU130_assertion wasDerivedFrom befree-20140225 NP826682.RABIbbH78Okw9tItxlcAlfEqcj7U5Lc9cJ2RGOse9a9IU130_provenance.
- NP826682.RABIbbH78Okw9tItxlcAlfEqcj7U5Lc9cJ2RGOse9a9IU130_assertion wasGeneratedBy ECO_0000203 NP826682.RABIbbH78Okw9tItxlcAlfEqcj7U5Lc9cJ2RGOse9a9IU130_provenance.