Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP463832.RAEBSk1ia0ETNfEqxLMVNbrF6nB9gbfkK20WOCBSBz-NA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP463832.RAEBSk1ia0ETNfEqxLMVNbrF6nB9gbfkK20WOCBSBz-NA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP463832.RAEBSk1ia0ETNfEqxLMVNbrF6nB9gbfkK20WOCBSBz-NA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP463832.RAEBSk1ia0ETNfEqxLMVNbrF6nB9gbfkK20WOCBSBz-NA130_provenance.
- NP463832.RAEBSk1ia0ETNfEqxLMVNbrF6nB9gbfkK20WOCBSBz-NA130_assertion description "[Two electrophoretic variants of haptoglobin in which the alpha 2 chain had more basic or more acidic spots were found in DMD patients with a rapidly progressing form of the disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP463832.RAEBSk1ia0ETNfEqxLMVNbrF6nB9gbfkK20WOCBSBz-NA130_provenance.
- NP463832.RAEBSk1ia0ETNfEqxLMVNbrF6nB9gbfkK20WOCBSBz-NA130_assertion evidence source_evidence_literature NP463832.RAEBSk1ia0ETNfEqxLMVNbrF6nB9gbfkK20WOCBSBz-NA130_provenance.
- NP463832.RAEBSk1ia0ETNfEqxLMVNbrF6nB9gbfkK20WOCBSBz-NA130_assertion SIO_000772 2776732 NP463832.RAEBSk1ia0ETNfEqxLMVNbrF6nB9gbfkK20WOCBSBz-NA130_provenance.
- NP463832.RAEBSk1ia0ETNfEqxLMVNbrF6nB9gbfkK20WOCBSBz-NA130_assertion wasDerivedFrom befree-20150227 NP463832.RAEBSk1ia0ETNfEqxLMVNbrF6nB9gbfkK20WOCBSBz-NA130_provenance.
- NP463832.RAEBSk1ia0ETNfEqxLMVNbrF6nB9gbfkK20WOCBSBz-NA130_assertion wasGeneratedBy ECO_0000203 NP463832.RAEBSk1ia0ETNfEqxLMVNbrF6nB9gbfkK20WOCBSBz-NA130_provenance.
- befree-20150227 importedOn "2015-02-27" NP463832.RAEBSk1ia0ETNfEqxLMVNbrF6nB9gbfkK20WOCBSBz-NA130_provenance.