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- source_evidence_literature type ECO_0000212 NP978356.RApnOTRin1MbrT98QfnkpZWex4Y6_y0Ke1BHXNxlLuI3g130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP978356.RApnOTRin1MbrT98QfnkpZWex4Y6_y0Ke1BHXNxlLuI3g130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP978356.RApnOTRin1MbrT98QfnkpZWex4Y6_y0Ke1BHXNxlLuI3g130_provenance.
- NP978356.RApnOTRin1MbrT98QfnkpZWex4Y6_y0Ke1BHXNxlLuI3g130_assertion description "[The syndrome of microcornea, myopic chorioretinal atrophy, and telecanthus (MMCAT) is caused by mutations in ADAMTS18.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP978356.RApnOTRin1MbrT98QfnkpZWex4Y6_y0Ke1BHXNxlLuI3g130_provenance.
- NP978356.RApnOTRin1MbrT98QfnkpZWex4Y6_y0Ke1BHXNxlLuI3g130_assertion evidence source_evidence_literature NP978356.RApnOTRin1MbrT98QfnkpZWex4Y6_y0Ke1BHXNxlLuI3g130_provenance.
- NP978356.RApnOTRin1MbrT98QfnkpZWex4Y6_y0Ke1BHXNxlLuI3g130_assertion SIO_000772 23818446 NP978356.RApnOTRin1MbrT98QfnkpZWex4Y6_y0Ke1BHXNxlLuI3g130_provenance.
- NP978356.RApnOTRin1MbrT98QfnkpZWex4Y6_y0Ke1BHXNxlLuI3g130_assertion wasDerivedFrom befree-20150227 NP978356.RApnOTRin1MbrT98QfnkpZWex4Y6_y0Ke1BHXNxlLuI3g130_provenance.
- NP978356.RApnOTRin1MbrT98QfnkpZWex4Y6_y0Ke1BHXNxlLuI3g130_assertion wasGeneratedBy ECO_0000203 NP978356.RApnOTRin1MbrT98QfnkpZWex4Y6_y0Ke1BHXNxlLuI3g130_provenance.
- befree-20150227 importedOn "2015-02-27" NP978356.RApnOTRin1MbrT98QfnkpZWex4Y6_y0Ke1BHXNxlLuI3g130_provenance.