Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP303477.RAm6l66Hnq7hprHdidDPaYS3f-EWFASKA8BvCQ7K0cWmk130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP303477.RAm6l66Hnq7hprHdidDPaYS3f-EWFASKA8BvCQ7K0cWmk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP303477.RAm6l66Hnq7hprHdidDPaYS3f-EWFASKA8BvCQ7K0cWmk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP303477.RAm6l66Hnq7hprHdidDPaYS3f-EWFASKA8BvCQ7K0cWmk130_provenance.
- NP303477.RAm6l66Hnq7hprHdidDPaYS3f-EWFASKA8BvCQ7K0cWmk130_assertion description "[No mutations were detected around the cytoplasmic domain of the gene in our patients, indicating that the mechanisms of clonal evolution to MDS/AML in patients with AA might be different from those with SCN.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP303477.RAm6l66Hnq7hprHdidDPaYS3f-EWFASKA8BvCQ7K0cWmk130_provenance.
- NP303477.RAm6l66Hnq7hprHdidDPaYS3f-EWFASKA8BvCQ7K0cWmk130_assertion evidence source_evidence_literature NP303477.RAm6l66Hnq7hprHdidDPaYS3f-EWFASKA8BvCQ7K0cWmk130_provenance.
- NP303477.RAm6l66Hnq7hprHdidDPaYS3f-EWFASKA8BvCQ7K0cWmk130_assertion SIO_000772 11122117 NP303477.RAm6l66Hnq7hprHdidDPaYS3f-EWFASKA8BvCQ7K0cWmk130_provenance.
- NP303477.RAm6l66Hnq7hprHdidDPaYS3f-EWFASKA8BvCQ7K0cWmk130_assertion wasDerivedFrom befree-2016 NP303477.RAm6l66Hnq7hprHdidDPaYS3f-EWFASKA8BvCQ7K0cWmk130_provenance.
- NP303477.RAm6l66Hnq7hprHdidDPaYS3f-EWFASKA8BvCQ7K0cWmk130_assertion wasGeneratedBy ECO_0000203 NP303477.RAm6l66Hnq7hprHdidDPaYS3f-EWFASKA8BvCQ7K0cWmk130_provenance.
- befree-2016 importedOn "2016-02-19" NP303477.RAm6l66Hnq7hprHdidDPaYS3f-EWFASKA8BvCQ7K0cWmk130_provenance.