Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP791343.RALTOUxmh9_n67_YdhFzWocwITojpzxW1JkdDoQgFl69A130_assertion> ?p ?o ?g. }
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- NP791343.RALTOUxmh9_n67_YdhFzWocwITojpzxW1JkdDoQgFl69A130_assertion type Assertion NP791343.RALTOUxmh9_n67_YdhFzWocwITojpzxW1JkdDoQgFl69A130_head.
- NP791343.RALTOUxmh9_n67_YdhFzWocwITojpzxW1JkdDoQgFl69A130_assertion description "[Recessive GJA1 mutations cause Hallermann-Streiff syndrome, a disorder showing substantial overlap with ODDD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP791343.RALTOUxmh9_n67_YdhFzWocwITojpzxW1JkdDoQgFl69A130_provenance.
- NP791343.RALTOUxmh9_n67_YdhFzWocwITojpzxW1JkdDoQgFl69A130_assertion evidence source_evidence_literature NP791343.RALTOUxmh9_n67_YdhFzWocwITojpzxW1JkdDoQgFl69A130_provenance.
- NP791343.RALTOUxmh9_n67_YdhFzWocwITojpzxW1JkdDoQgFl69A130_assertion SIO_000772 21871435 NP791343.RALTOUxmh9_n67_YdhFzWocwITojpzxW1JkdDoQgFl69A130_provenance.
- NP791343.RALTOUxmh9_n67_YdhFzWocwITojpzxW1JkdDoQgFl69A130_assertion wasDerivedFrom befree-20140225 NP791343.RALTOUxmh9_n67_YdhFzWocwITojpzxW1JkdDoQgFl69A130_provenance.
- NP791343.RALTOUxmh9_n67_YdhFzWocwITojpzxW1JkdDoQgFl69A130_assertion wasGeneratedBy ECO_0000203 NP791343.RALTOUxmh9_n67_YdhFzWocwITojpzxW1JkdDoQgFl69A130_provenance.