Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP443768.RAIOd7O77DjgDsWxnJ5MyrmCGZIc6dqY4oRs-YHq0I5xs130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP443768.RAIOd7O77DjgDsWxnJ5MyrmCGZIc6dqY4oRs-YHq0I5xs130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP443768.RAIOd7O77DjgDsWxnJ5MyrmCGZIc6dqY4oRs-YHq0I5xs130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP443768.RAIOd7O77DjgDsWxnJ5MyrmCGZIc6dqY4oRs-YHq0I5xs130_provenance.
- NP443768.RAIOd7O77DjgDsWxnJ5MyrmCGZIc6dqY4oRs-YHq0I5xs130_assertion description "[Comparison of these data with the available genetic and physical maps of 17p12 --> p11 shows that this region, which is frequently subject to rearrangement-inducing diseases, such as Smith-Magenis syndrome, Charcot-Marie-Tooth type 1A, and HNPP, presents recombination hot spots.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP443768.RAIOd7O77DjgDsWxnJ5MyrmCGZIc6dqY4oRs-YHq0I5xs130_provenance.
- NP443768.RAIOd7O77DjgDsWxnJ5MyrmCGZIc6dqY4oRs-YHq0I5xs130_assertion evidence source_evidence_literature NP443768.RAIOd7O77DjgDsWxnJ5MyrmCGZIc6dqY4oRs-YHq0I5xs130_provenance.
- NP443768.RAIOd7O77DjgDsWxnJ5MyrmCGZIc6dqY4oRs-YHq0I5xs130_assertion SIO_000772 8565626 NP443768.RAIOd7O77DjgDsWxnJ5MyrmCGZIc6dqY4oRs-YHq0I5xs130_provenance.
- NP443768.RAIOd7O77DjgDsWxnJ5MyrmCGZIc6dqY4oRs-YHq0I5xs130_assertion wasDerivedFrom befree-20140225 NP443768.RAIOd7O77DjgDsWxnJ5MyrmCGZIc6dqY4oRs-YHq0I5xs130_provenance.
- NP443768.RAIOd7O77DjgDsWxnJ5MyrmCGZIc6dqY4oRs-YHq0I5xs130_assertion wasGeneratedBy ECO_0000203 NP443768.RAIOd7O77DjgDsWxnJ5MyrmCGZIc6dqY4oRs-YHq0I5xs130_provenance.
- befree-20140225 importedOn "2014-02-25" NP443768.RAIOd7O77DjgDsWxnJ5MyrmCGZIc6dqY4oRs-YHq0I5xs130_provenance.