Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP340522.RADnKOXWmfSvJ7lU0Cnvo2kPuNk8ocOq1tTitHSOeBOZA130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP340522.RADnKOXWmfSvJ7lU0Cnvo2kPuNk8ocOq1tTitHSOeBOZA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP340522.RADnKOXWmfSvJ7lU0Cnvo2kPuNk8ocOq1tTitHSOeBOZA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP340522.RADnKOXWmfSvJ7lU0Cnvo2kPuNk8ocOq1tTitHSOeBOZA130_provenance.
- NP340522.RADnKOXWmfSvJ7lU0Cnvo2kPuNk8ocOq1tTitHSOeBOZA130_assertion description "[We have performed linkage analysis in a large French-Acadian kindred segregating one form of autosomal dominant Charcot-Marie-Tooth disease (CMTD) (type IA) using 17 polymorphic DNA markers spanning human chromosome 17 and demonstrate linkage to several markers in the pericentromeric region, including DNA probes pA10-41, EW301, S12-30, pTH17.19, c11-2B, and p11-2c11.5.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP340522.RADnKOXWmfSvJ7lU0Cnvo2kPuNk8ocOq1tTitHSOeBOZA130_provenance.
- NP340522.RADnKOXWmfSvJ7lU0Cnvo2kPuNk8ocOq1tTitHSOeBOZA130_assertion evidence source_evidence_literature NP340522.RADnKOXWmfSvJ7lU0Cnvo2kPuNk8ocOq1tTitHSOeBOZA130_provenance.
- NP340522.RADnKOXWmfSvJ7lU0Cnvo2kPuNk8ocOq1tTitHSOeBOZA130_assertion SIO_000772 2316525 NP340522.RADnKOXWmfSvJ7lU0Cnvo2kPuNk8ocOq1tTitHSOeBOZA130_provenance.
- NP340522.RADnKOXWmfSvJ7lU0Cnvo2kPuNk8ocOq1tTitHSOeBOZA130_assertion wasDerivedFrom befree-20140225 NP340522.RADnKOXWmfSvJ7lU0Cnvo2kPuNk8ocOq1tTitHSOeBOZA130_provenance.
- NP340522.RADnKOXWmfSvJ7lU0Cnvo2kPuNk8ocOq1tTitHSOeBOZA130_assertion wasGeneratedBy ECO_0000203 NP340522.RADnKOXWmfSvJ7lU0Cnvo2kPuNk8ocOq1tTitHSOeBOZA130_provenance.
- befree-20140225 importedOn "2014-02-25" NP340522.RADnKOXWmfSvJ7lU0Cnvo2kPuNk8ocOq1tTitHSOeBOZA130_provenance.