Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP544269.RAjQ_bTinAmNmCOCqOxtXN6oP2eRMyN4bu5ysbsSTvLMg130_assertion> ?p ?o ?g. }
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- NP544269.RAjQ_bTinAmNmCOCqOxtXN6oP2eRMyN4bu5ysbsSTvLMg130_assertion type Assertion NP544269.RAjQ_bTinAmNmCOCqOxtXN6oP2eRMyN4bu5ysbsSTvLMg130_head.
- NP544269.RAjQ_bTinAmNmCOCqOxtXN6oP2eRMyN4bu5ysbsSTvLMg130_assertion description "[Mutations at a single codon in Mad homology 2 domain of SMAD4 cause Myhre syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP544269.RAjQ_bTinAmNmCOCqOxtXN6oP2eRMyN4bu5ysbsSTvLMg130_provenance.
- NP544269.RAjQ_bTinAmNmCOCqOxtXN6oP2eRMyN4bu5ysbsSTvLMg130_assertion evidence source_evidence_literature NP544269.RAjQ_bTinAmNmCOCqOxtXN6oP2eRMyN4bu5ysbsSTvLMg130_provenance.
- NP544269.RAjQ_bTinAmNmCOCqOxtXN6oP2eRMyN4bu5ysbsSTvLMg130_assertion SIO_000772 22158539 NP544269.RAjQ_bTinAmNmCOCqOxtXN6oP2eRMyN4bu5ysbsSTvLMg130_provenance.
- NP544269.RAjQ_bTinAmNmCOCqOxtXN6oP2eRMyN4bu5ysbsSTvLMg130_assertion wasDerivedFrom befree-20150227 NP544269.RAjQ_bTinAmNmCOCqOxtXN6oP2eRMyN4bu5ysbsSTvLMg130_provenance.
- NP544269.RAjQ_bTinAmNmCOCqOxtXN6oP2eRMyN4bu5ysbsSTvLMg130_assertion wasGeneratedBy ECO_0000203 NP544269.RAjQ_bTinAmNmCOCqOxtXN6oP2eRMyN4bu5ysbsSTvLMg130_provenance.