Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP945969.RAypw_uXyUn0MiCDYnbBNgnvJGBKzmFzldyvnm2inGEww130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP945969.RAypw_uXyUn0MiCDYnbBNgnvJGBKzmFzldyvnm2inGEww130_assertion type Assertion NP945969.RAypw_uXyUn0MiCDYnbBNgnvJGBKzmFzldyvnm2inGEww130_head.
- NP945969.RAypw_uXyUn0MiCDYnbBNgnvJGBKzmFzldyvnm2inGEww130_assertion description "[Mutation screening and DNA sequencing of the MET gene, which is mapped to 7q31, revealed only the presence of simple sequence polymorphisms but no apparent acquired disease-associated mutations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP945969.RAypw_uXyUn0MiCDYnbBNgnvJGBKzmFzldyvnm2inGEww130_provenance.
- NP945969.RAypw_uXyUn0MiCDYnbBNgnvJGBKzmFzldyvnm2inGEww130_assertion evidence source_evidence_literature NP945969.RAypw_uXyUn0MiCDYnbBNgnvJGBKzmFzldyvnm2inGEww130_provenance.
- NP945969.RAypw_uXyUn0MiCDYnbBNgnvJGBKzmFzldyvnm2inGEww130_assertion SIO_000772 9485032 NP945969.RAypw_uXyUn0MiCDYnbBNgnvJGBKzmFzldyvnm2inGEww130_provenance.
- NP945969.RAypw_uXyUn0MiCDYnbBNgnvJGBKzmFzldyvnm2inGEww130_assertion wasDerivedFrom befree-20150227 NP945969.RAypw_uXyUn0MiCDYnbBNgnvJGBKzmFzldyvnm2inGEww130_provenance.
- NP945969.RAypw_uXyUn0MiCDYnbBNgnvJGBKzmFzldyvnm2inGEww130_assertion wasGeneratedBy ECO_0000203 NP945969.RAypw_uXyUn0MiCDYnbBNgnvJGBKzmFzldyvnm2inGEww130_provenance.