Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP456076.RAPP1iFkiimJXE9O970mdOYnyFhw-RZCefPSbjO0xS2Kc130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP456076.RAPP1iFkiimJXE9O970mdOYnyFhw-RZCefPSbjO0xS2Kc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP456076.RAPP1iFkiimJXE9O970mdOYnyFhw-RZCefPSbjO0xS2Kc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP456076.RAPP1iFkiimJXE9O970mdOYnyFhw-RZCefPSbjO0xS2Kc130_provenance.
- NP456076.RAPP1iFkiimJXE9O970mdOYnyFhw-RZCefPSbjO0xS2Kc130_assertion description "[Fibrodysplasia ossificans progressiva (FOP; OMIM 135100) is a rare heritable disorder of connective tissue characterized by congenital malformations of the great toes and recurrent episodes of painful soft tissue swelling that lead to heterotopic ossifications.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP456076.RAPP1iFkiimJXE9O970mdOYnyFhw-RZCefPSbjO0xS2Kc130_provenance.
- NP456076.RAPP1iFkiimJXE9O970mdOYnyFhw-RZCefPSbjO0xS2Kc130_assertion evidence source_evidence_literature NP456076.RAPP1iFkiimJXE9O970mdOYnyFhw-RZCefPSbjO0xS2Kc130_provenance.
- NP456076.RAPP1iFkiimJXE9O970mdOYnyFhw-RZCefPSbjO0xS2Kc130_assertion SIO_000772 19300893 NP456076.RAPP1iFkiimJXE9O970mdOYnyFhw-RZCefPSbjO0xS2Kc130_provenance.
- NP456076.RAPP1iFkiimJXE9O970mdOYnyFhw-RZCefPSbjO0xS2Kc130_assertion wasDerivedFrom befree-20140225 NP456076.RAPP1iFkiimJXE9O970mdOYnyFhw-RZCefPSbjO0xS2Kc130_provenance.
- NP456076.RAPP1iFkiimJXE9O970mdOYnyFhw-RZCefPSbjO0xS2Kc130_assertion wasGeneratedBy ECO_0000203 NP456076.RAPP1iFkiimJXE9O970mdOYnyFhw-RZCefPSbjO0xS2Kc130_provenance.
- befree-20140225 importedOn "2014-02-25" NP456076.RAPP1iFkiimJXE9O970mdOYnyFhw-RZCefPSbjO0xS2Kc130_provenance.