Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP933159.RAxwyrZbW0JCq5eg7hvZrNUZ-eIZESJ4hin7et5gdRPz4130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP933159.RAxwyrZbW0JCq5eg7hvZrNUZ-eIZESJ4hin7et5gdRPz4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP933159.RAxwyrZbW0JCq5eg7hvZrNUZ-eIZESJ4hin7et5gdRPz4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP933159.RAxwyrZbW0JCq5eg7hvZrNUZ-eIZESJ4hin7et5gdRPz4130_provenance.
- NP933159.RAxwyrZbW0JCq5eg7hvZrNUZ-eIZESJ4hin7et5gdRPz4130_assertion description "[AFG3L2 forms either a homo-oligomeric isoenzyme or a hetero-oligomeric complex with paraplegin, a homologous protein mutated in hereditary spastic paraplegia type 7 (SPG7).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP933159.RAxwyrZbW0JCq5eg7hvZrNUZ-eIZESJ4hin7et5gdRPz4130_provenance.
- NP933159.RAxwyrZbW0JCq5eg7hvZrNUZ-eIZESJ4hin7et5gdRPz4130_assertion evidence source_evidence_literature NP933159.RAxwyrZbW0JCq5eg7hvZrNUZ-eIZESJ4hin7et5gdRPz4130_provenance.
- NP933159.RAxwyrZbW0JCq5eg7hvZrNUZ-eIZESJ4hin7et5gdRPz4130_assertion SIO_000772 22022284 NP933159.RAxwyrZbW0JCq5eg7hvZrNUZ-eIZESJ4hin7et5gdRPz4130_provenance.
- NP933159.RAxwyrZbW0JCq5eg7hvZrNUZ-eIZESJ4hin7et5gdRPz4130_assertion wasDerivedFrom befree-2016 NP933159.RAxwyrZbW0JCq5eg7hvZrNUZ-eIZESJ4hin7et5gdRPz4130_provenance.
- NP933159.RAxwyrZbW0JCq5eg7hvZrNUZ-eIZESJ4hin7et5gdRPz4130_assertion wasGeneratedBy ECO_0000203 NP933159.RAxwyrZbW0JCq5eg7hvZrNUZ-eIZESJ4hin7et5gdRPz4130_provenance.
- befree-2016 importedOn "2016-02-19" NP933159.RAxwyrZbW0JCq5eg7hvZrNUZ-eIZESJ4hin7et5gdRPz4130_provenance.