Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP213034.RAhl394gmAiuzs-X6zlAE06HO1jSs3dDuQwlD0zL0I490130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP213034.RAhl394gmAiuzs-X6zlAE06HO1jSs3dDuQwlD0zL0I490130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP213034.RAhl394gmAiuzs-X6zlAE06HO1jSs3dDuQwlD0zL0I490130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP213034.RAhl394gmAiuzs-X6zlAE06HO1jSs3dDuQwlD0zL0I490130_provenance.
- NP213034.RAhl394gmAiuzs-X6zlAE06HO1jSs3dDuQwlD0zL0I490130_assertion description "[The study revealed that 4 genotypes (- -(SEA)/ -alpha(3.7), - -(SA)/-alpha(3.7), - -(SEA)/-alpha(3.7 Sallanches), - -alpha(3.7)/-alpha(3.7 Sallanches)) were responsible for Hb H disease, the alpha+ thalassemia mutation (-alpha(3.7) deletion) being the most common defect.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP213034.RAhl394gmAiuzs-X6zlAE06HO1jSs3dDuQwlD0zL0I490130_provenance.
- NP213034.RAhl394gmAiuzs-X6zlAE06HO1jSs3dDuQwlD0zL0I490130_assertion evidence source_evidence_literature NP213034.RAhl394gmAiuzs-X6zlAE06HO1jSs3dDuQwlD0zL0I490130_provenance.
- NP213034.RAhl394gmAiuzs-X6zlAE06HO1jSs3dDuQwlD0zL0I490130_assertion SIO_000772 20154289 NP213034.RAhl394gmAiuzs-X6zlAE06HO1jSs3dDuQwlD0zL0I490130_provenance.
- NP213034.RAhl394gmAiuzs-X6zlAE06HO1jSs3dDuQwlD0zL0I490130_assertion wasDerivedFrom befree-20140225 NP213034.RAhl394gmAiuzs-X6zlAE06HO1jSs3dDuQwlD0zL0I490130_provenance.
- NP213034.RAhl394gmAiuzs-X6zlAE06HO1jSs3dDuQwlD0zL0I490130_assertion wasGeneratedBy ECO_0000203 NP213034.RAhl394gmAiuzs-X6zlAE06HO1jSs3dDuQwlD0zL0I490130_provenance.
- befree-20140225 importedOn "2014-02-25" NP213034.RAhl394gmAiuzs-X6zlAE06HO1jSs3dDuQwlD0zL0I490130_provenance.