Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP604362.RA8pXf2yFgCpA3uTtv2XHZbSmBl3SBnUp_-FEOkE7Z1BY130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP604362.RA8pXf2yFgCpA3uTtv2XHZbSmBl3SBnUp_-FEOkE7Z1BY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP604362.RA8pXf2yFgCpA3uTtv2XHZbSmBl3SBnUp_-FEOkE7Z1BY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP604362.RA8pXf2yFgCpA3uTtv2XHZbSmBl3SBnUp_-FEOkE7Z1BY130_provenance.
- NP604362.RA8pXf2yFgCpA3uTtv2XHZbSmBl3SBnUp_-FEOkE7Z1BY130_assertion description "[Using DNA samples obtained from two unrelated patients, diagnosed as having familial dysalbuminaemic hyperthyroxinaemia (FDH), exons 1-14 which span the entire coding region of the human serum albumin (HSA) gene were amplified by the polymerase chain reaction.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP604362.RA8pXf2yFgCpA3uTtv2XHZbSmBl3SBnUp_-FEOkE7Z1BY130_provenance.
- NP604362.RA8pXf2yFgCpA3uTtv2XHZbSmBl3SBnUp_-FEOkE7Z1BY130_assertion evidence source_evidence_literature NP604362.RA8pXf2yFgCpA3uTtv2XHZbSmBl3SBnUp_-FEOkE7Z1BY130_provenance.
- NP604362.RA8pXf2yFgCpA3uTtv2XHZbSmBl3SBnUp_-FEOkE7Z1BY130_assertion SIO_000772 8064810 NP604362.RA8pXf2yFgCpA3uTtv2XHZbSmBl3SBnUp_-FEOkE7Z1BY130_provenance.
- NP604362.RA8pXf2yFgCpA3uTtv2XHZbSmBl3SBnUp_-FEOkE7Z1BY130_assertion wasDerivedFrom befree-20150227 NP604362.RA8pXf2yFgCpA3uTtv2XHZbSmBl3SBnUp_-FEOkE7Z1BY130_provenance.
- NP604362.RA8pXf2yFgCpA3uTtv2XHZbSmBl3SBnUp_-FEOkE7Z1BY130_assertion wasGeneratedBy ECO_0000203 NP604362.RA8pXf2yFgCpA3uTtv2XHZbSmBl3SBnUp_-FEOkE7Z1BY130_provenance.
- befree-20150227 importedOn "2015-02-27" NP604362.RA8pXf2yFgCpA3uTtv2XHZbSmBl3SBnUp_-FEOkE7Z1BY130_provenance.