Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP978736.RASm1AMPhOejjUV5JZ1wFMl0qvOIdVE2vCHJdfJZc00a0130_assertion> ?p ?o ?g. }
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- NP978736.RASm1AMPhOejjUV5JZ1wFMl0qvOIdVE2vCHJdfJZc00a0130_assertion type Assertion NP978736.RASm1AMPhOejjUV5JZ1wFMl0qvOIdVE2vCHJdfJZc00a0130_head.
- NP978736.RASm1AMPhOejjUV5JZ1wFMl0qvOIdVE2vCHJdfJZc00a0130_assertion description "[Split hand/split foot malformation (SHFM; ectrodactyly) is genetically heterogeneous, with mutations identified at five loci (SHFM1 at 7q21.3, SHFM2 at Xq26, SHFM3 at 10q24, SHFM4 at 3q27 and SHFM5 at 2q31).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP978736.RASm1AMPhOejjUV5JZ1wFMl0qvOIdVE2vCHJdfJZc00a0130_provenance.
- NP978736.RASm1AMPhOejjUV5JZ1wFMl0qvOIdVE2vCHJdfJZc00a0130_assertion evidence source_evidence_literature NP978736.RASm1AMPhOejjUV5JZ1wFMl0qvOIdVE2vCHJdfJZc00a0130_provenance.
- NP978736.RASm1AMPhOejjUV5JZ1wFMl0qvOIdVE2vCHJdfJZc00a0130_assertion SIO_000772 15232212 NP978736.RASm1AMPhOejjUV5JZ1wFMl0qvOIdVE2vCHJdfJZc00a0130_provenance.
- NP978736.RASm1AMPhOejjUV5JZ1wFMl0qvOIdVE2vCHJdfJZc00a0130_assertion wasDerivedFrom befree-20150227 NP978736.RASm1AMPhOejjUV5JZ1wFMl0qvOIdVE2vCHJdfJZc00a0130_provenance.
- NP978736.RASm1AMPhOejjUV5JZ1wFMl0qvOIdVE2vCHJdfJZc00a0130_assertion wasGeneratedBy ECO_0000203 NP978736.RASm1AMPhOejjUV5JZ1wFMl0qvOIdVE2vCHJdfJZc00a0130_provenance.