Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1345926.RAmMy1rMcYp5ouewsZ36szrVDpyGiosEWcAGpTBTCaDEg130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1345926.RAmMy1rMcYp5ouewsZ36szrVDpyGiosEWcAGpTBTCaDEg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1345926.RAmMy1rMcYp5ouewsZ36szrVDpyGiosEWcAGpTBTCaDEg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1345926.RAmMy1rMcYp5ouewsZ36szrVDpyGiosEWcAGpTBTCaDEg130_provenance.
- NP1345926.RAmMy1rMcYp5ouewsZ36szrVDpyGiosEWcAGpTBTCaDEg130_assertion description "[Using these STR markers, we found that the deletion coincided with the CMT1A/HNPP monomer unit in eight of the nine families.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1345926.RAmMy1rMcYp5ouewsZ36szrVDpyGiosEWcAGpTBTCaDEg130_provenance.
- NP1345926.RAmMy1rMcYp5ouewsZ36szrVDpyGiosEWcAGpTBTCaDEg130_assertion evidence source_evidence_literature NP1345926.RAmMy1rMcYp5ouewsZ36szrVDpyGiosEWcAGpTBTCaDEg130_provenance.
- NP1345926.RAmMy1rMcYp5ouewsZ36szrVDpyGiosEWcAGpTBTCaDEg130_assertion SIO_000772 8565626 NP1345926.RAmMy1rMcYp5ouewsZ36szrVDpyGiosEWcAGpTBTCaDEg130_provenance.
- NP1345926.RAmMy1rMcYp5ouewsZ36szrVDpyGiosEWcAGpTBTCaDEg130_assertion wasDerivedFrom befree-2016 NP1345926.RAmMy1rMcYp5ouewsZ36szrVDpyGiosEWcAGpTBTCaDEg130_provenance.
- NP1345926.RAmMy1rMcYp5ouewsZ36szrVDpyGiosEWcAGpTBTCaDEg130_assertion wasGeneratedBy ECO_0000203 NP1345926.RAmMy1rMcYp5ouewsZ36szrVDpyGiosEWcAGpTBTCaDEg130_provenance.
- befree-2016 importedOn "2016-02-19" NP1345926.RAmMy1rMcYp5ouewsZ36szrVDpyGiosEWcAGpTBTCaDEg130_provenance.