Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP418660.RA4rfnAu1wexQ-KAmFPovuQGVa_hWj7HbRH7HqMuHE5q0130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP418660.RA4rfnAu1wexQ-KAmFPovuQGVa_hWj7HbRH7HqMuHE5q0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP418660.RA4rfnAu1wexQ-KAmFPovuQGVa_hWj7HbRH7HqMuHE5q0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP418660.RA4rfnAu1wexQ-KAmFPovuQGVa_hWj7HbRH7HqMuHE5q0130_provenance.
- NP418660.RA4rfnAu1wexQ-KAmFPovuQGVa_hWj7HbRH7HqMuHE5q0130_assertion description "[Three novel mutations in SQSTM1 identified in familial Paget's disease of bone.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP418660.RA4rfnAu1wexQ-KAmFPovuQGVa_hWj7HbRH7HqMuHE5q0130_provenance.
- NP418660.RA4rfnAu1wexQ-KAmFPovuQGVa_hWj7HbRH7HqMuHE5q0130_assertion evidence source_evidence_literature NP418660.RA4rfnAu1wexQ-KAmFPovuQGVa_hWj7HbRH7HqMuHE5q0130_provenance.
- NP418660.RA4rfnAu1wexQ-KAmFPovuQGVa_hWj7HbRH7HqMuHE5q0130_assertion SIO_000772 14584883 NP418660.RA4rfnAu1wexQ-KAmFPovuQGVa_hWj7HbRH7HqMuHE5q0130_provenance.
- NP418660.RA4rfnAu1wexQ-KAmFPovuQGVa_hWj7HbRH7HqMuHE5q0130_assertion wasDerivedFrom befree-2016 NP418660.RA4rfnAu1wexQ-KAmFPovuQGVa_hWj7HbRH7HqMuHE5q0130_provenance.
- NP418660.RA4rfnAu1wexQ-KAmFPovuQGVa_hWj7HbRH7HqMuHE5q0130_assertion wasGeneratedBy ECO_0000203 NP418660.RA4rfnAu1wexQ-KAmFPovuQGVa_hWj7HbRH7HqMuHE5q0130_provenance.
- befree-2016 importedOn "2016-02-19" NP418660.RA4rfnAu1wexQ-KAmFPovuQGVa_hWj7HbRH7HqMuHE5q0130_provenance.