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- source_evidence_literature type ECO_0000212 NP1293577.RABRn-w3hJMvJIswUjUntyHfjGAM9Qo7xWk9dxvq3Zcaw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1293577.RABRn-w3hJMvJIswUjUntyHfjGAM9Qo7xWk9dxvq3Zcaw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1293577.RABRn-w3hJMvJIswUjUntyHfjGAM9Qo7xWk9dxvq3Zcaw130_provenance.
- NP1293577.RABRn-w3hJMvJIswUjUntyHfjGAM9Qo7xWk9dxvq3Zcaw130_assertion description "[Variants of unknown significance occurred most frequently in FBN1 and were associated with greater curve severity, systemic features of Marfan syndrome, and joint hypermobility.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1293577.RABRn-w3hJMvJIswUjUntyHfjGAM9Qo7xWk9dxvq3Zcaw130_provenance.
- NP1293577.RABRn-w3hJMvJIswUjUntyHfjGAM9Qo7xWk9dxvq3Zcaw130_assertion evidence source_evidence_literature NP1293577.RABRn-w3hJMvJIswUjUntyHfjGAM9Qo7xWk9dxvq3Zcaw130_provenance.
- NP1293577.RABRn-w3hJMvJIswUjUntyHfjGAM9Qo7xWk9dxvq3Zcaw130_assertion SIO_000772 26333736 NP1293577.RABRn-w3hJMvJIswUjUntyHfjGAM9Qo7xWk9dxvq3Zcaw130_provenance.
- NP1293577.RABRn-w3hJMvJIswUjUntyHfjGAM9Qo7xWk9dxvq3Zcaw130_assertion wasDerivedFrom befree-2016 NP1293577.RABRn-w3hJMvJIswUjUntyHfjGAM9Qo7xWk9dxvq3Zcaw130_provenance.
- NP1293577.RABRn-w3hJMvJIswUjUntyHfjGAM9Qo7xWk9dxvq3Zcaw130_assertion wasGeneratedBy ECO_0000203 NP1293577.RABRn-w3hJMvJIswUjUntyHfjGAM9Qo7xWk9dxvq3Zcaw130_provenance.
- befree-2016 importedOn "2016-02-19" NP1293577.RABRn-w3hJMvJIswUjUntyHfjGAM9Qo7xWk9dxvq3Zcaw130_provenance.