Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP883741.RAewyOPJTK17OeLq5GNSG-ZQeEaLjTjn0XghvXcXYaPf0130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP883741.RAewyOPJTK17OeLq5GNSG-ZQeEaLjTjn0XghvXcXYaPf0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP883741.RAewyOPJTK17OeLq5GNSG-ZQeEaLjTjn0XghvXcXYaPf0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP883741.RAewyOPJTK17OeLq5GNSG-ZQeEaLjTjn0XghvXcXYaPf0130_provenance.
- NP883741.RAewyOPJTK17OeLq5GNSG-ZQeEaLjTjn0XghvXcXYaPf0130_assertion wasGeneratedBy ECO_0000203 NP883741.RAewyOPJTK17OeLq5GNSG-ZQeEaLjTjn0XghvXcXYaPf0130_provenance.
- NP883741.RAewyOPJTK17OeLq5GNSG-ZQeEaLjTjn0XghvXcXYaPf0130_assertion wasDerivedFrom befree-20140225 NP883741.RAewyOPJTK17OeLq5GNSG-ZQeEaLjTjn0XghvXcXYaPf0130_provenance.
- NP883741.RAewyOPJTK17OeLq5GNSG-ZQeEaLjTjn0XghvXcXYaPf0130_assertion SIO_000772 9408592 NP883741.RAewyOPJTK17OeLq5GNSG-ZQeEaLjTjn0XghvXcXYaPf0130_provenance.
- NP883741.RAewyOPJTK17OeLq5GNSG-ZQeEaLjTjn0XghvXcXYaPf0130_assertion evidence source_evidence_literature NP883741.RAewyOPJTK17OeLq5GNSG-ZQeEaLjTjn0XghvXcXYaPf0130_provenance.
- NP883741.RAewyOPJTK17OeLq5GNSG-ZQeEaLjTjn0XghvXcXYaPf0130_assertion description "[We analyzed a 1.5-Mb duplication of the p11.2-12 region of chromosome 17, including the PMP-22 gene (CMT1A duplication), seven families with Charcot-Marie-Tooth disease type I (CMT I) and six sporadic patients with suspected CMT I by Southern blot analysis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP883741.RAewyOPJTK17OeLq5GNSG-ZQeEaLjTjn0XghvXcXYaPf0130_provenance.
- befree-20140225 importedOn "2014-02-25" NP883741.RAewyOPJTK17OeLq5GNSG-ZQeEaLjTjn0XghvXcXYaPf0130_provenance.