Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP945969.RAypw_uXyUn0MiCDYnbBNgnvJGBKzmFzldyvnm2inGEww130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP945969.RAypw_uXyUn0MiCDYnbBNgnvJGBKzmFzldyvnm2inGEww130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP945969.RAypw_uXyUn0MiCDYnbBNgnvJGBKzmFzldyvnm2inGEww130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP945969.RAypw_uXyUn0MiCDYnbBNgnvJGBKzmFzldyvnm2inGEww130_provenance.
- 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.
- befree-20150227 importedOn "2015-02-27" NP945969.RAypw_uXyUn0MiCDYnbBNgnvJGBKzmFzldyvnm2inGEww130_provenance.