Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP791343.RALTOUxmh9_n67_YdhFzWocwITojpzxW1JkdDoQgFl69A130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP791343.RALTOUxmh9_n67_YdhFzWocwITojpzxW1JkdDoQgFl69A130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP791343.RALTOUxmh9_n67_YdhFzWocwITojpzxW1JkdDoQgFl69A130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP791343.RALTOUxmh9_n67_YdhFzWocwITojpzxW1JkdDoQgFl69A130_provenance.
- 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.
- befree-20140225 importedOn "2014-02-25" NP791343.RALTOUxmh9_n67_YdhFzWocwITojpzxW1JkdDoQgFl69A130_provenance.