Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP179628.RANFECGqfBgC92IhrAtYMCrwlt1wx2lOegncEe5ibHvcI130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP179628.RANFECGqfBgC92IhrAtYMCrwlt1wx2lOegncEe5ibHvcI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP179628.RANFECGqfBgC92IhrAtYMCrwlt1wx2lOegncEe5ibHvcI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP179628.RANFECGqfBgC92IhrAtYMCrwlt1wx2lOegncEe5ibHvcI130_provenance.
- NP179628.RANFECGqfBgC92IhrAtYMCrwlt1wx2lOegncEe5ibHvcI130_assertion description "[The multiplex ligation-dependent probe amplification (MLPA) method was used to analyze 118 DNA samples from 90 alpha-thalassemia (alpha-thal) patients and 28 normal persons from Southern China, where the main causes of alpha-thal are three large deletions (-alpha3.7, -alpha4.2, and --SEA) and two point mutations in the alpha-globin gene cluster on chromosome 16.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP179628.RANFECGqfBgC92IhrAtYMCrwlt1wx2lOegncEe5ibHvcI130_provenance.
- NP179628.RANFECGqfBgC92IhrAtYMCrwlt1wx2lOegncEe5ibHvcI130_assertion evidence source_evidence_literature NP179628.RANFECGqfBgC92IhrAtYMCrwlt1wx2lOegncEe5ibHvcI130_provenance.
- NP179628.RANFECGqfBgC92IhrAtYMCrwlt1wx2lOegncEe5ibHvcI130_assertion SIO_000772 19065334 NP179628.RANFECGqfBgC92IhrAtYMCrwlt1wx2lOegncEe5ibHvcI130_provenance.
- NP179628.RANFECGqfBgC92IhrAtYMCrwlt1wx2lOegncEe5ibHvcI130_assertion wasDerivedFrom befree-20140225 NP179628.RANFECGqfBgC92IhrAtYMCrwlt1wx2lOegncEe5ibHvcI130_provenance.
- NP179628.RANFECGqfBgC92IhrAtYMCrwlt1wx2lOegncEe5ibHvcI130_assertion wasGeneratedBy ECO_0000203 NP179628.RANFECGqfBgC92IhrAtYMCrwlt1wx2lOegncEe5ibHvcI130_provenance.
- befree-20140225 importedOn "2014-02-25" NP179628.RANFECGqfBgC92IhrAtYMCrwlt1wx2lOegncEe5ibHvcI130_provenance.