Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP787231.RAKnJNpR1DcwOyCAIoy6V4TEsHu0iXRNDSxw_VjXOkD0M130_assertion> ?p ?o ?g. }
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- NP787231.RAKnJNpR1DcwOyCAIoy6V4TEsHu0iXRNDSxw_VjXOkD0M130_assertion type Assertion NP787231.RAKnJNpR1DcwOyCAIoy6V4TEsHu0iXRNDSxw_VjXOkD0M130_head.
- NP787231.RAKnJNpR1DcwOyCAIoy6V4TEsHu0iXRNDSxw_VjXOkD0M130_assertion description "[Based on these observations, an autosomal dominant form of ectrodactyly is assumed to reside in this region and the locus has been designated SHFD1 (split hand/split foot disorder).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP787231.RAKnJNpR1DcwOyCAIoy6V4TEsHu0iXRNDSxw_VjXOkD0M130_provenance.
- NP787231.RAKnJNpR1DcwOyCAIoy6V4TEsHu0iXRNDSxw_VjXOkD0M130_assertion evidence source_evidence_literature NP787231.RAKnJNpR1DcwOyCAIoy6V4TEsHu0iXRNDSxw_VjXOkD0M130_provenance.
- NP787231.RAKnJNpR1DcwOyCAIoy6V4TEsHu0iXRNDSxw_VjXOkD0M130_assertion SIO_000772 7987314 NP787231.RAKnJNpR1DcwOyCAIoy6V4TEsHu0iXRNDSxw_VjXOkD0M130_provenance.
- NP787231.RAKnJNpR1DcwOyCAIoy6V4TEsHu0iXRNDSxw_VjXOkD0M130_assertion wasDerivedFrom befree-20150227 NP787231.RAKnJNpR1DcwOyCAIoy6V4TEsHu0iXRNDSxw_VjXOkD0M130_provenance.
- NP787231.RAKnJNpR1DcwOyCAIoy6V4TEsHu0iXRNDSxw_VjXOkD0M130_assertion wasGeneratedBy ECO_0000203 NP787231.RAKnJNpR1DcwOyCAIoy6V4TEsHu0iXRNDSxw_VjXOkD0M130_provenance.