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- source_evidence_literature type ECO_0000212 NP549305.RAwyxCibj6Nk7K69TO4lx5iLNADga82FiH1AXXkjBLa-I130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP549305.RAwyxCibj6Nk7K69TO4lx5iLNADga82FiH1AXXkjBLa-I130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP549305.RAwyxCibj6Nk7K69TO4lx5iLNADga82FiH1AXXkjBLa-I130_provenance.
- NP549305.RAwyxCibj6Nk7K69TO4lx5iLNADga82FiH1AXXkjBLa-I130_assertion description "[If no causative ENG or ACVRL1 mutation is found, proband samples are referred for sequence analysis of MADH4 (associated with a combined syndrome of juvenile polyposis and HHT).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP549305.RAwyxCibj6Nk7K69TO4lx5iLNADga82FiH1AXXkjBLa-I130_provenance.
- NP549305.RAwyxCibj6Nk7K69TO4lx5iLNADga82FiH1AXXkjBLa-I130_assertion evidence source_evidence_literature NP549305.RAwyxCibj6Nk7K69TO4lx5iLNADga82FiH1AXXkjBLa-I130_provenance.
- NP549305.RAwyxCibj6Nk7K69TO4lx5iLNADga82FiH1AXXkjBLa-I130_assertion SIO_000772 16690726 NP549305.RAwyxCibj6Nk7K69TO4lx5iLNADga82FiH1AXXkjBLa-I130_provenance.
- NP549305.RAwyxCibj6Nk7K69TO4lx5iLNADga82FiH1AXXkjBLa-I130_assertion wasDerivedFrom befree-2016 NP549305.RAwyxCibj6Nk7K69TO4lx5iLNADga82FiH1AXXkjBLa-I130_provenance.
- NP549305.RAwyxCibj6Nk7K69TO4lx5iLNADga82FiH1AXXkjBLa-I130_assertion wasGeneratedBy ECO_0000203 NP549305.RAwyxCibj6Nk7K69TO4lx5iLNADga82FiH1AXXkjBLa-I130_provenance.
- befree-2016 importedOn "2016-02-19" NP549305.RAwyxCibj6Nk7K69TO4lx5iLNADga82FiH1AXXkjBLa-I130_provenance.