Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP724144.RAXMD8dLelhDtVXUU_uh9ei0EEF3eLtMlYBXIFDH6dIW8130_assertion> ?p ?o ?g. }
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- NP724144.RAXMD8dLelhDtVXUU_uh9ei0EEF3eLtMlYBXIFDH6dIW8130_assertion type Assertion NP724144.RAXMD8dLelhDtVXUU_uh9ei0EEF3eLtMlYBXIFDH6dIW8130_head.
- NP724144.RAXMD8dLelhDtVXUU_uh9ei0EEF3eLtMlYBXIFDH6dIW8130_assertion wasGeneratedBy ECO_0000203 NP724144.RAXMD8dLelhDtVXUU_uh9ei0EEF3eLtMlYBXIFDH6dIW8130_provenance.
- NP724144.RAXMD8dLelhDtVXUU_uh9ei0EEF3eLtMlYBXIFDH6dIW8130_assertion wasDerivedFrom befree-20150227 NP724144.RAXMD8dLelhDtVXUU_uh9ei0EEF3eLtMlYBXIFDH6dIW8130_provenance.
- NP724144.RAXMD8dLelhDtVXUU_uh9ei0EEF3eLtMlYBXIFDH6dIW8130_assertion SIO_000772 16332960 NP724144.RAXMD8dLelhDtVXUU_uh9ei0EEF3eLtMlYBXIFDH6dIW8130_provenance.
- NP724144.RAXMD8dLelhDtVXUU_uh9ei0EEF3eLtMlYBXIFDH6dIW8130_assertion evidence source_evidence_literature NP724144.RAXMD8dLelhDtVXUU_uh9ei0EEF3eLtMlYBXIFDH6dIW8130_provenance.
- NP724144.RAXMD8dLelhDtVXUU_uh9ei0EEF3eLtMlYBXIFDH6dIW8130_assertion description "[Various mutations in the TBX5 gene have been identified in patients with Holt-Oram syndrome, which is characterized by congenital defects in the heart and upper extremities.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP724144.RAXMD8dLelhDtVXUU_uh9ei0EEF3eLtMlYBXIFDH6dIW8130_provenance.