Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP186655.RAHwC46I1YYxcreOiypgdqvclNetYPYS0tsc-eO9Fpnpo130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP186655.RAHwC46I1YYxcreOiypgdqvclNetYPYS0tsc-eO9Fpnpo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP186655.RAHwC46I1YYxcreOiypgdqvclNetYPYS0tsc-eO9Fpnpo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP186655.RAHwC46I1YYxcreOiypgdqvclNetYPYS0tsc-eO9Fpnpo130_provenance.
- NP186655.RAHwC46I1YYxcreOiypgdqvclNetYPYS0tsc-eO9Fpnpo130_assertion description "[Mutations in the SOS1 are associated with Noonan syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP186655.RAHwC46I1YYxcreOiypgdqvclNetYPYS0tsc-eO9Fpnpo130_provenance.
- NP186655.RAHwC46I1YYxcreOiypgdqvclNetYPYS0tsc-eO9Fpnpo130_assertion evidence source_evidence_literature NP186655.RAHwC46I1YYxcreOiypgdqvclNetYPYS0tsc-eO9Fpnpo130_provenance.
- NP186655.RAHwC46I1YYxcreOiypgdqvclNetYPYS0tsc-eO9Fpnpo130_assertion SIO_000772 19020799 NP186655.RAHwC46I1YYxcreOiypgdqvclNetYPYS0tsc-eO9Fpnpo130_provenance.
- NP186655.RAHwC46I1YYxcreOiypgdqvclNetYPYS0tsc-eO9Fpnpo130_assertion wasDerivedFrom lhgdn-20090331 NP186655.RAHwC46I1YYxcreOiypgdqvclNetYPYS0tsc-eO9Fpnpo130_provenance.
- NP186655.RAHwC46I1YYxcreOiypgdqvclNetYPYS0tsc-eO9Fpnpo130_assertion wasGeneratedBy ECO_0000203 NP186655.RAHwC46I1YYxcreOiypgdqvclNetYPYS0tsc-eO9Fpnpo130_provenance.
- lhgdn-20090331 importedOn "2009-03-31" NP186655.RAHwC46I1YYxcreOiypgdqvclNetYPYS0tsc-eO9Fpnpo130_provenance.