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- source_evidence_literature type ECO_0000212 NP933165.RA-OmqujbjCEPS7RE8vZfenac5NNZpJwyfxUgvvdaw3UI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP933165.RA-OmqujbjCEPS7RE8vZfenac5NNZpJwyfxUgvvdaw3UI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP933165.RA-OmqujbjCEPS7RE8vZfenac5NNZpJwyfxUgvvdaw3UI130_provenance.
- NP933165.RA-OmqujbjCEPS7RE8vZfenac5NNZpJwyfxUgvvdaw3UI130_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." NP933165.RA-OmqujbjCEPS7RE8vZfenac5NNZpJwyfxUgvvdaw3UI130_provenance.
- NP933165.RA-OmqujbjCEPS7RE8vZfenac5NNZpJwyfxUgvvdaw3UI130_assertion evidence source_evidence_literature NP933165.RA-OmqujbjCEPS7RE8vZfenac5NNZpJwyfxUgvvdaw3UI130_provenance.
- NP933165.RA-OmqujbjCEPS7RE8vZfenac5NNZpJwyfxUgvvdaw3UI130_assertion SIO_000772 22022284 NP933165.RA-OmqujbjCEPS7RE8vZfenac5NNZpJwyfxUgvvdaw3UI130_provenance.
- NP933165.RA-OmqujbjCEPS7RE8vZfenac5NNZpJwyfxUgvvdaw3UI130_assertion wasDerivedFrom befree-2016 NP933165.RA-OmqujbjCEPS7RE8vZfenac5NNZpJwyfxUgvvdaw3UI130_provenance.
- NP933165.RA-OmqujbjCEPS7RE8vZfenac5NNZpJwyfxUgvvdaw3UI130_assertion wasGeneratedBy ECO_0000203 NP933165.RA-OmqujbjCEPS7RE8vZfenac5NNZpJwyfxUgvvdaw3UI130_provenance.
- befree-2016 importedOn "2016-02-19" NP933165.RA-OmqujbjCEPS7RE8vZfenac5NNZpJwyfxUgvvdaw3UI130_provenance.