Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP168650.RAtzo3frzaksgp2Np0kCb3i9EIlU1ab2Q2OfNWPt9lE7A130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP168650.RAtzo3frzaksgp2Np0kCb3i9EIlU1ab2Q2OfNWPt9lE7A130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP168650.RAtzo3frzaksgp2Np0kCb3i9EIlU1ab2Q2OfNWPt9lE7A130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP168650.RAtzo3frzaksgp2Np0kCb3i9EIlU1ab2Q2OfNWPt9lE7A130_provenance.
- NP168650.RAtzo3frzaksgp2Np0kCb3i9EIlU1ab2Q2OfNWPt9lE7A130_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." NP168650.RAtzo3frzaksgp2Np0kCb3i9EIlU1ab2Q2OfNWPt9lE7A130_provenance.
- NP168650.RAtzo3frzaksgp2Np0kCb3i9EIlU1ab2Q2OfNWPt9lE7A130_assertion evidence source_evidence_literature NP168650.RAtzo3frzaksgp2Np0kCb3i9EIlU1ab2Q2OfNWPt9lE7A130_provenance.
- NP168650.RAtzo3frzaksgp2Np0kCb3i9EIlU1ab2Q2OfNWPt9lE7A130_assertion SIO_000772 8565626 NP168650.RAtzo3frzaksgp2Np0kCb3i9EIlU1ab2Q2OfNWPt9lE7A130_provenance.
- NP168650.RAtzo3frzaksgp2Np0kCb3i9EIlU1ab2Q2OfNWPt9lE7A130_assertion wasDerivedFrom befree-20140225 NP168650.RAtzo3frzaksgp2Np0kCb3i9EIlU1ab2Q2OfNWPt9lE7A130_provenance.
- NP168650.RAtzo3frzaksgp2Np0kCb3i9EIlU1ab2Q2OfNWPt9lE7A130_assertion wasGeneratedBy ECO_0000203 NP168650.RAtzo3frzaksgp2Np0kCb3i9EIlU1ab2Q2OfNWPt9lE7A130_provenance.
- befree-20140225 importedOn "2014-02-25" NP168650.RAtzo3frzaksgp2Np0kCb3i9EIlU1ab2Q2OfNWPt9lE7A130_provenance.