Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP736387.RA1s0kolOar-aBJlvVll302fJJmFyZFkCCx1rLy_ItFiM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP736387.RA1s0kolOar-aBJlvVll302fJJmFyZFkCCx1rLy_ItFiM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP736387.RA1s0kolOar-aBJlvVll302fJJmFyZFkCCx1rLy_ItFiM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP736387.RA1s0kolOar-aBJlvVll302fJJmFyZFkCCx1rLy_ItFiM130_provenance.
- NP736387.RA1s0kolOar-aBJlvVll302fJJmFyZFkCCx1rLy_ItFiM130_assertion description "[Patients in whom no mutation is identified through this mutation protocol, may be sub-cohorts representing a different FAP pathogenesis including MYH associated polyposis and somatic cell mosaicism for APC gene mutations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP736387.RA1s0kolOar-aBJlvVll302fJJmFyZFkCCx1rLy_ItFiM130_provenance.
- NP736387.RA1s0kolOar-aBJlvVll302fJJmFyZFkCCx1rLy_ItFiM130_assertion evidence source_evidence_literature NP736387.RA1s0kolOar-aBJlvVll302fJJmFyZFkCCx1rLy_ItFiM130_provenance.
- NP736387.RA1s0kolOar-aBJlvVll302fJJmFyZFkCCx1rLy_ItFiM130_assertion SIO_000772 19414146 NP736387.RA1s0kolOar-aBJlvVll302fJJmFyZFkCCx1rLy_ItFiM130_provenance.
- NP736387.RA1s0kolOar-aBJlvVll302fJJmFyZFkCCx1rLy_ItFiM130_assertion wasDerivedFrom befree-2016 NP736387.RA1s0kolOar-aBJlvVll302fJJmFyZFkCCx1rLy_ItFiM130_provenance.
- NP736387.RA1s0kolOar-aBJlvVll302fJJmFyZFkCCx1rLy_ItFiM130_assertion wasGeneratedBy ECO_0000203 NP736387.RA1s0kolOar-aBJlvVll302fJJmFyZFkCCx1rLy_ItFiM130_provenance.
- befree-2016 importedOn "2016-02-19" NP736387.RA1s0kolOar-aBJlvVll302fJJmFyZFkCCx1rLy_ItFiM130_provenance.