Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP276856.RA2AcmV3hitf7jQbepn_-pRpRmlS4wxnUuM1RDHLE1XC4130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP276856.RA2AcmV3hitf7jQbepn_-pRpRmlS4wxnUuM1RDHLE1XC4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP276856.RA2AcmV3hitf7jQbepn_-pRpRmlS4wxnUuM1RDHLE1XC4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP276856.RA2AcmV3hitf7jQbepn_-pRpRmlS4wxnUuM1RDHLE1XC4130_provenance.
- NP276856.RA2AcmV3hitf7jQbepn_-pRpRmlS4wxnUuM1RDHLE1XC4130_assertion description "[Here, sequence analysis of the 17 exons of SPG4 in 87 unrelated AD-HSP patients has resulted in the detection of 34 novel mutations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP276856.RA2AcmV3hitf7jQbepn_-pRpRmlS4wxnUuM1RDHLE1XC4130_provenance.
- NP276856.RA2AcmV3hitf7jQbepn_-pRpRmlS4wxnUuM1RDHLE1XC4130_assertion evidence source_evidence_literature NP276856.RA2AcmV3hitf7jQbepn_-pRpRmlS4wxnUuM1RDHLE1XC4130_provenance.
- NP276856.RA2AcmV3hitf7jQbepn_-pRpRmlS4wxnUuM1RDHLE1XC4130_assertion SIO_000772 10699187 NP276856.RA2AcmV3hitf7jQbepn_-pRpRmlS4wxnUuM1RDHLE1XC4130_provenance.
- NP276856.RA2AcmV3hitf7jQbepn_-pRpRmlS4wxnUuM1RDHLE1XC4130_assertion wasDerivedFrom befree-2016 NP276856.RA2AcmV3hitf7jQbepn_-pRpRmlS4wxnUuM1RDHLE1XC4130_provenance.
- NP276856.RA2AcmV3hitf7jQbepn_-pRpRmlS4wxnUuM1RDHLE1XC4130_assertion wasGeneratedBy ECO_0000203 NP276856.RA2AcmV3hitf7jQbepn_-pRpRmlS4wxnUuM1RDHLE1XC4130_provenance.
- befree-2016 importedOn "2016-02-19" NP276856.RA2AcmV3hitf7jQbepn_-pRpRmlS4wxnUuM1RDHLE1XC4130_provenance.