Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP874165.RAkL7RN3QkX5qW1hHVnOlzIBQ4b3UDLaE5FoQev8VGFX0130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP874165.RAkL7RN3QkX5qW1hHVnOlzIBQ4b3UDLaE5FoQev8VGFX0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP874165.RAkL7RN3QkX5qW1hHVnOlzIBQ4b3UDLaE5FoQev8VGFX0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP874165.RAkL7RN3QkX5qW1hHVnOlzIBQ4b3UDLaE5FoQev8VGFX0130_provenance.
- NP874165.RAkL7RN3QkX5qW1hHVnOlzIBQ4b3UDLaE5FoQev8VGFX0130_assertion description "[reported 24 patients from 19 Brazilian families with 17?-hydroxylase deficiency and showed that p.W406R and p.R362C corresponded to 50% and 32% of CYP17A1 mutant alleles, respectively.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP874165.RAkL7RN3QkX5qW1hHVnOlzIBQ4b3UDLaE5FoQev8VGFX0130_provenance.
- NP874165.RAkL7RN3QkX5qW1hHVnOlzIBQ4b3UDLaE5FoQev8VGFX0130_assertion evidence source_evidence_literature NP874165.RAkL7RN3QkX5qW1hHVnOlzIBQ4b3UDLaE5FoQev8VGFX0130_provenance.
- NP874165.RAkL7RN3QkX5qW1hHVnOlzIBQ4b3UDLaE5FoQev8VGFX0130_assertion SIO_000772 21340157 NP874165.RAkL7RN3QkX5qW1hHVnOlzIBQ4b3UDLaE5FoQev8VGFX0130_provenance.
- NP874165.RAkL7RN3QkX5qW1hHVnOlzIBQ4b3UDLaE5FoQev8VGFX0130_assertion wasDerivedFrom befree-2016 NP874165.RAkL7RN3QkX5qW1hHVnOlzIBQ4b3UDLaE5FoQev8VGFX0130_provenance.
- NP874165.RAkL7RN3QkX5qW1hHVnOlzIBQ4b3UDLaE5FoQev8VGFX0130_assertion wasGeneratedBy ECO_0000203 NP874165.RAkL7RN3QkX5qW1hHVnOlzIBQ4b3UDLaE5FoQev8VGFX0130_provenance.
- befree-2016 importedOn "2016-02-19" NP874165.RAkL7RN3QkX5qW1hHVnOlzIBQ4b3UDLaE5FoQev8VGFX0130_provenance.