Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1011705.RAS6mCXgDVR7vuMMECTQ8Y2uAtxQDIJk25mEtnoqLjq_s130_assertion> ?p ?o ?g. }
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- NP1011705.RAS6mCXgDVR7vuMMECTQ8Y2uAtxQDIJk25mEtnoqLjq_s130_assertion type Assertion NP1011705.RAS6mCXgDVR7vuMMECTQ8Y2uAtxQDIJk25mEtnoqLjq_s130_head.
- NP1011705.RAS6mCXgDVR7vuMMECTQ8Y2uAtxQDIJk25mEtnoqLjq_s130_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." NP1011705.RAS6mCXgDVR7vuMMECTQ8Y2uAtxQDIJk25mEtnoqLjq_s130_provenance.
- NP1011705.RAS6mCXgDVR7vuMMECTQ8Y2uAtxQDIJk25mEtnoqLjq_s130_assertion evidence source_evidence_literature NP1011705.RAS6mCXgDVR7vuMMECTQ8Y2uAtxQDIJk25mEtnoqLjq_s130_provenance.
- NP1011705.RAS6mCXgDVR7vuMMECTQ8Y2uAtxQDIJk25mEtnoqLjq_s130_assertion SIO_000772 15232212 NP1011705.RAS6mCXgDVR7vuMMECTQ8Y2uAtxQDIJk25mEtnoqLjq_s130_provenance.
- NP1011705.RAS6mCXgDVR7vuMMECTQ8Y2uAtxQDIJk25mEtnoqLjq_s130_assertion wasDerivedFrom befree-20150227 NP1011705.RAS6mCXgDVR7vuMMECTQ8Y2uAtxQDIJk25mEtnoqLjq_s130_provenance.
- NP1011705.RAS6mCXgDVR7vuMMECTQ8Y2uAtxQDIJk25mEtnoqLjq_s130_assertion wasGeneratedBy ECO_0000203 NP1011705.RAS6mCXgDVR7vuMMECTQ8Y2uAtxQDIJk25mEtnoqLjq_s130_provenance.