Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1245965.RAH4HiwBswjurDSo7XQxXAFuDcNns3WCA-ngq2RFt1kKU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1245965.RAH4HiwBswjurDSo7XQxXAFuDcNns3WCA-ngq2RFt1kKU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1245965.RAH4HiwBswjurDSo7XQxXAFuDcNns3WCA-ngq2RFt1kKU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1245965.RAH4HiwBswjurDSo7XQxXAFuDcNns3WCA-ngq2RFt1kKU130_provenance.
- NP1245965.RAH4HiwBswjurDSo7XQxXAFuDcNns3WCA-ngq2RFt1kKU130_assertion description "[This study demonstrates that harboring HSP90-SUMO1 identifies healthy individuals at risk for plasma cell dyscrasias and that dominant inheritance of posttranslationally modified autoantigenic paratargs is one of the strongest molecular defined risk factors for MGUS, MM, and WM.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1245965.RAH4HiwBswjurDSo7XQxXAFuDcNns3WCA-ngq2RFt1kKU130_provenance.
- NP1245965.RAH4HiwBswjurDSo7XQxXAFuDcNns3WCA-ngq2RFt1kKU130_assertion evidence source_evidence_literature NP1245965.RAH4HiwBswjurDSo7XQxXAFuDcNns3WCA-ngq2RFt1kKU130_provenance.
- NP1245965.RAH4HiwBswjurDSo7XQxXAFuDcNns3WCA-ngq2RFt1kKU130_assertion SIO_000772 25485683 NP1245965.RAH4HiwBswjurDSo7XQxXAFuDcNns3WCA-ngq2RFt1kKU130_provenance.
- NP1245965.RAH4HiwBswjurDSo7XQxXAFuDcNns3WCA-ngq2RFt1kKU130_assertion wasDerivedFrom befree-2016 NP1245965.RAH4HiwBswjurDSo7XQxXAFuDcNns3WCA-ngq2RFt1kKU130_provenance.
- NP1245965.RAH4HiwBswjurDSo7XQxXAFuDcNns3WCA-ngq2RFt1kKU130_assertion wasGeneratedBy ECO_0000203 NP1245965.RAH4HiwBswjurDSo7XQxXAFuDcNns3WCA-ngq2RFt1kKU130_provenance.
- befree-2016 importedOn "2016-02-19" NP1245965.RAH4HiwBswjurDSo7XQxXAFuDcNns3WCA-ngq2RFt1kKU130_provenance.