Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP252781.RAdHqu1Eg1TO2fOh4hwss0j_b9VNyF4ARgM8dv9-JlRec130_assertion> ?p ?o ?g. }
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- NP252781.RAdHqu1Eg1TO2fOh4hwss0j_b9VNyF4ARgM8dv9-JlRec130_assertion type Assertion NP252781.RAdHqu1Eg1TO2fOh4hwss0j_b9VNyF4ARgM8dv9-JlRec130_head.
- NP252781.RAdHqu1Eg1TO2fOh4hwss0j_b9VNyF4ARgM8dv9-JlRec130_assertion description "[The spectrum of mutations in TBX3: Genotype/Phenotype relationship in ulnar-mammary syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP252781.RAdHqu1Eg1TO2fOh4hwss0j_b9VNyF4ARgM8dv9-JlRec130_provenance.
- NP252781.RAdHqu1Eg1TO2fOh4hwss0j_b9VNyF4ARgM8dv9-JlRec130_assertion evidence source_evidence_literature NP252781.RAdHqu1Eg1TO2fOh4hwss0j_b9VNyF4ARgM8dv9-JlRec130_provenance.
- NP252781.RAdHqu1Eg1TO2fOh4hwss0j_b9VNyF4ARgM8dv9-JlRec130_assertion SIO_000772 10330342 NP252781.RAdHqu1Eg1TO2fOh4hwss0j_b9VNyF4ARgM8dv9-JlRec130_provenance.
- NP252781.RAdHqu1Eg1TO2fOh4hwss0j_b9VNyF4ARgM8dv9-JlRec130_assertion wasDerivedFrom befree-2016 NP252781.RAdHqu1Eg1TO2fOh4hwss0j_b9VNyF4ARgM8dv9-JlRec130_provenance.
- NP252781.RAdHqu1Eg1TO2fOh4hwss0j_b9VNyF4ARgM8dv9-JlRec130_assertion wasGeneratedBy ECO_0000203 NP252781.RAdHqu1Eg1TO2fOh4hwss0j_b9VNyF4ARgM8dv9-JlRec130_provenance.