Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1410105.RAeOp2CzD_DTU192mwUA9GA6cv1e6gQ1R4DwGwUQjm7g8130_assertion> ?p ?o ?g. }
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- NP1410105.RAeOp2CzD_DTU192mwUA9GA6cv1e6gQ1R4DwGwUQjm7g8130_assertion type Assertion NP1410105.RAeOp2CzD_DTU192mwUA9GA6cv1e6gQ1R4DwGwUQjm7g8130_head.
- NP1410105.RAeOp2CzD_DTU192mwUA9GA6cv1e6gQ1R4DwGwUQjm7g8130_assertion description "[A third family cosegregates mild mitral valve prolapse syndrome with a mutation in FBN1 that can be functionally distinguished from those associated with the classic MFS phenotype.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1410105.RAeOp2CzD_DTU192mwUA9GA6cv1e6gQ1R4DwGwUQjm7g8130_provenance.
- NP1410105.RAeOp2CzD_DTU192mwUA9GA6cv1e6gQ1R4DwGwUQjm7g8130_assertion evidence source_evidence_literature NP1410105.RAeOp2CzD_DTU192mwUA9GA6cv1e6gQ1R4DwGwUQjm7g8130_provenance.
- NP1410105.RAeOp2CzD_DTU192mwUA9GA6cv1e6gQ1R4DwGwUQjm7g8130_assertion SIO_000772 9837823 NP1410105.RAeOp2CzD_DTU192mwUA9GA6cv1e6gQ1R4DwGwUQjm7g8130_provenance.
- NP1410105.RAeOp2CzD_DTU192mwUA9GA6cv1e6gQ1R4DwGwUQjm7g8130_assertion wasDerivedFrom befree-2016 NP1410105.RAeOp2CzD_DTU192mwUA9GA6cv1e6gQ1R4DwGwUQjm7g8130_provenance.
- NP1410105.RAeOp2CzD_DTU192mwUA9GA6cv1e6gQ1R4DwGwUQjm7g8130_assertion wasGeneratedBy ECO_0000203 NP1410105.RAeOp2CzD_DTU192mwUA9GA6cv1e6gQ1R4DwGwUQjm7g8130_provenance.