Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP924670.RAUT68N5roW1LoCSHUgcRQ6HrVS6xHz_Nmx8F086X4tbY130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP924670.RAUT68N5roW1LoCSHUgcRQ6HrVS6xHz_Nmx8F086X4tbY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP924670.RAUT68N5roW1LoCSHUgcRQ6HrVS6xHz_Nmx8F086X4tbY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP924670.RAUT68N5roW1LoCSHUgcRQ6HrVS6xHz_Nmx8F086X4tbY130_provenance.
- NP924670.RAUT68N5roW1LoCSHUgcRQ6HrVS6xHz_Nmx8F086X4tbY130_assertion description "[In this report we describe a novel SOD1 mutation (Gly147Ser) in an Italian sporadic ALS patient.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP924670.RAUT68N5roW1LoCSHUgcRQ6HrVS6xHz_Nmx8F086X4tbY130_provenance.
- NP924670.RAUT68N5roW1LoCSHUgcRQ6HrVS6xHz_Nmx8F086X4tbY130_assertion evidence source_evidence_literature NP924670.RAUT68N5roW1LoCSHUgcRQ6HrVS6xHz_Nmx8F086X4tbY130_provenance.
- NP924670.RAUT68N5roW1LoCSHUgcRQ6HrVS6xHz_Nmx8F086X4tbY130_assertion SIO_000772 21929355 NP924670.RAUT68N5roW1LoCSHUgcRQ6HrVS6xHz_Nmx8F086X4tbY130_provenance.
- NP924670.RAUT68N5roW1LoCSHUgcRQ6HrVS6xHz_Nmx8F086X4tbY130_assertion wasDerivedFrom befree-2016 NP924670.RAUT68N5roW1LoCSHUgcRQ6HrVS6xHz_Nmx8F086X4tbY130_provenance.
- NP924670.RAUT68N5roW1LoCSHUgcRQ6HrVS6xHz_Nmx8F086X4tbY130_assertion wasGeneratedBy ECO_0000203 NP924670.RAUT68N5roW1LoCSHUgcRQ6HrVS6xHz_Nmx8F086X4tbY130_provenance.
- befree-2016 importedOn "2016-02-19" NP924670.RAUT68N5roW1LoCSHUgcRQ6HrVS6xHz_Nmx8F086X4tbY130_provenance.