Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP410361.RADM9PhLJHdj5rVvGUXjxKT7e9sOikNQt_mX2qsSRBsiQ130_assertion> ?p ?o ?g. }
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- NP410361.RADM9PhLJHdj5rVvGUXjxKT7e9sOikNQt_mX2qsSRBsiQ130_assertion type Assertion NP410361.RADM9PhLJHdj5rVvGUXjxKT7e9sOikNQt_mX2qsSRBsiQ130_head.
- NP410361.RADM9PhLJHdj5rVvGUXjxKT7e9sOikNQt_mX2qsSRBsiQ130_assertion description "[However, the absence of MSX2 mutations in some of the FPP patients analysed and the presence of FPP associated with chromosome 11p deletions in DEFECT 11 (OMIM 601224) patients or associated with Saethre-Chotzen syndrome suggests genetic heterogeneity for this disorder.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP410361.RADM9PhLJHdj5rVvGUXjxKT7e9sOikNQt_mX2qsSRBsiQ130_provenance.
- NP410361.RADM9PhLJHdj5rVvGUXjxKT7e9sOikNQt_mX2qsSRBsiQ130_assertion evidence source_evidence_literature NP410361.RADM9PhLJHdj5rVvGUXjxKT7e9sOikNQt_mX2qsSRBsiQ130_provenance.
- NP410361.RADM9PhLJHdj5rVvGUXjxKT7e9sOikNQt_mX2qsSRBsiQ130_assertion SIO_000772 11106354 NP410361.RADM9PhLJHdj5rVvGUXjxKT7e9sOikNQt_mX2qsSRBsiQ130_provenance.
- NP410361.RADM9PhLJHdj5rVvGUXjxKT7e9sOikNQt_mX2qsSRBsiQ130_assertion wasDerivedFrom befree-20140225 NP410361.RADM9PhLJHdj5rVvGUXjxKT7e9sOikNQt_mX2qsSRBsiQ130_provenance.
- NP410361.RADM9PhLJHdj5rVvGUXjxKT7e9sOikNQt_mX2qsSRBsiQ130_assertion wasGeneratedBy ECO_0000203 NP410361.RADM9PhLJHdj5rVvGUXjxKT7e9sOikNQt_mX2qsSRBsiQ130_provenance.