Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP890807.RA93nsP_zcs4bynKqoqxYEbhFSoBMU7evI-F_DX2yCeb0130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP890807.RA93nsP_zcs4bynKqoqxYEbhFSoBMU7evI-F_DX2yCeb0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP890807.RA93nsP_zcs4bynKqoqxYEbhFSoBMU7evI-F_DX2yCeb0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP890807.RA93nsP_zcs4bynKqoqxYEbhFSoBMU7evI-F_DX2yCeb0130_provenance.
- befree-2016 importedOn "2016-02-19" NP890807.RA93nsP_zcs4bynKqoqxYEbhFSoBMU7evI-F_DX2yCeb0130_provenance.
- NP890807.RA93nsP_zcs4bynKqoqxYEbhFSoBMU7evI-F_DX2yCeb0130_assertion wasGeneratedBy ECO_0000203 NP890807.RA93nsP_zcs4bynKqoqxYEbhFSoBMU7evI-F_DX2yCeb0130_provenance.
- NP890807.RA93nsP_zcs4bynKqoqxYEbhFSoBMU7evI-F_DX2yCeb0130_assertion wasDerivedFrom befree-2016 NP890807.RA93nsP_zcs4bynKqoqxYEbhFSoBMU7evI-F_DX2yCeb0130_provenance.
- NP890807.RA93nsP_zcs4bynKqoqxYEbhFSoBMU7evI-F_DX2yCeb0130_assertion SIO_000772 21533187 NP890807.RA93nsP_zcs4bynKqoqxYEbhFSoBMU7evI-F_DX2yCeb0130_provenance.
- NP890807.RA93nsP_zcs4bynKqoqxYEbhFSoBMU7evI-F_DX2yCeb0130_assertion evidence source_evidence_literature NP890807.RA93nsP_zcs4bynKqoqxYEbhFSoBMU7evI-F_DX2yCeb0130_provenance.
- NP890807.RA93nsP_zcs4bynKqoqxYEbhFSoBMU7evI-F_DX2yCeb0130_assertion description "[MC is clinically distinct from other multiple exostosis or multiple enchondromatosis syndromes and is unlinked to EXT1 and EXT2, the genes responsible for autosomal dominant multiple osteochondromas (MO).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP890807.RA93nsP_zcs4bynKqoqxYEbhFSoBMU7evI-F_DX2yCeb0130_provenance.