Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP545053.RAbJzwHEcshNy8hiGvwuzB2KmKyHs0Cl9R7fHymtfDges130_assertion> ?p ?o ?g. }
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- NP545053.RAbJzwHEcshNy8hiGvwuzB2KmKyHs0Cl9R7fHymtfDges130_assertion type Assertion NP545053.RAbJzwHEcshNy8hiGvwuzB2KmKyHs0Cl9R7fHymtfDges130_head.
- NP545053.RAbJzwHEcshNy8hiGvwuzB2KmKyHs0Cl9R7fHymtfDges130_assertion description "[In recent years, through a variety of mouse mutants that carry multigene and single gene mutations, we have learned that mutation in a single gene, Tbx1, is responsible for most of the congenital defects seen in the mouse models and in patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP545053.RAbJzwHEcshNy8hiGvwuzB2KmKyHs0Cl9R7fHymtfDges130_provenance.
- NP545053.RAbJzwHEcshNy8hiGvwuzB2KmKyHs0Cl9R7fHymtfDges130_assertion evidence source_evidence_literature NP545053.RAbJzwHEcshNy8hiGvwuzB2KmKyHs0Cl9R7fHymtfDges130_provenance.
- NP545053.RAbJzwHEcshNy8hiGvwuzB2KmKyHs0Cl9R7fHymtfDges130_assertion SIO_000772 16616724 NP545053.RAbJzwHEcshNy8hiGvwuzB2KmKyHs0Cl9R7fHymtfDges130_provenance.
- NP545053.RAbJzwHEcshNy8hiGvwuzB2KmKyHs0Cl9R7fHymtfDges130_assertion wasDerivedFrom befree-2016 NP545053.RAbJzwHEcshNy8hiGvwuzB2KmKyHs0Cl9R7fHymtfDges130_provenance.
- NP545053.RAbJzwHEcshNy8hiGvwuzB2KmKyHs0Cl9R7fHymtfDges130_assertion wasGeneratedBy ECO_0000203 NP545053.RAbJzwHEcshNy8hiGvwuzB2KmKyHs0Cl9R7fHymtfDges130_provenance.