Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP748557.RA9BXuc40T_C3RYzut6iW_uPjaKwZGoJWN_lJkN9ZeHSc130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP748557.RA9BXuc40T_C3RYzut6iW_uPjaKwZGoJWN_lJkN9ZeHSc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP748557.RA9BXuc40T_C3RYzut6iW_uPjaKwZGoJWN_lJkN9ZeHSc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP748557.RA9BXuc40T_C3RYzut6iW_uPjaKwZGoJWN_lJkN9ZeHSc130_provenance.
- befree-20150227 importedOn "2015-02-27" NP748557.RA9BXuc40T_C3RYzut6iW_uPjaKwZGoJWN_lJkN9ZeHSc130_provenance.
- NP748557.RA9BXuc40T_C3RYzut6iW_uPjaKwZGoJWN_lJkN9ZeHSc130_assertion wasGeneratedBy ECO_0000203 NP748557.RA9BXuc40T_C3RYzut6iW_uPjaKwZGoJWN_lJkN9ZeHSc130_provenance.
- NP748557.RA9BXuc40T_C3RYzut6iW_uPjaKwZGoJWN_lJkN9ZeHSc130_assertion wasDerivedFrom befree-20150227 NP748557.RA9BXuc40T_C3RYzut6iW_uPjaKwZGoJWN_lJkN9ZeHSc130_provenance.
- NP748557.RA9BXuc40T_C3RYzut6iW_uPjaKwZGoJWN_lJkN9ZeHSc130_assertion SIO_000772 23850728 NP748557.RA9BXuc40T_C3RYzut6iW_uPjaKwZGoJWN_lJkN9ZeHSc130_provenance.
- NP748557.RA9BXuc40T_C3RYzut6iW_uPjaKwZGoJWN_lJkN9ZeHSc130_assertion evidence source_evidence_literature NP748557.RA9BXuc40T_C3RYzut6iW_uPjaKwZGoJWN_lJkN9ZeHSc130_provenance.
- NP748557.RA9BXuc40T_C3RYzut6iW_uPjaKwZGoJWN_lJkN9ZeHSc130_assertion description "[A novel TNNI2 mutation causes Freeman-Sheldon syndrome in a Chinese family with an affected adult with only facial contractures.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP748557.RA9BXuc40T_C3RYzut6iW_uPjaKwZGoJWN_lJkN9ZeHSc130_provenance.