Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP380786.RAc09lddiC8IWcA2_DKegUyYRHBGXS2Mdl8vB51sn-rao130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP380786.RAc09lddiC8IWcA2_DKegUyYRHBGXS2Mdl8vB51sn-rao130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP380786.RAc09lddiC8IWcA2_DKegUyYRHBGXS2Mdl8vB51sn-rao130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP380786.RAc09lddiC8IWcA2_DKegUyYRHBGXS2Mdl8vB51sn-rao130_provenance.
- NP380786.RAc09lddiC8IWcA2_DKegUyYRHBGXS2Mdl8vB51sn-rao130_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." NP380786.RAc09lddiC8IWcA2_DKegUyYRHBGXS2Mdl8vB51sn-rao130_provenance.
- NP380786.RAc09lddiC8IWcA2_DKegUyYRHBGXS2Mdl8vB51sn-rao130_assertion evidence source_evidence_literature NP380786.RAc09lddiC8IWcA2_DKegUyYRHBGXS2Mdl8vB51sn-rao130_provenance.
- NP380786.RAc09lddiC8IWcA2_DKegUyYRHBGXS2Mdl8vB51sn-rao130_assertion SIO_000772 22022284 NP380786.RAc09lddiC8IWcA2_DKegUyYRHBGXS2Mdl8vB51sn-rao130_provenance.
- NP380786.RAc09lddiC8IWcA2_DKegUyYRHBGXS2Mdl8vB51sn-rao130_assertion wasDerivedFrom befree-20140225 NP380786.RAc09lddiC8IWcA2_DKegUyYRHBGXS2Mdl8vB51sn-rao130_provenance.
- NP380786.RAc09lddiC8IWcA2_DKegUyYRHBGXS2Mdl8vB51sn-rao130_assertion wasGeneratedBy ECO_0000203 NP380786.RAc09lddiC8IWcA2_DKegUyYRHBGXS2Mdl8vB51sn-rao130_provenance.
- befree-20140225 importedOn "2014-02-25" NP380786.RAc09lddiC8IWcA2_DKegUyYRHBGXS2Mdl8vB51sn-rao130_provenance.