Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP151867.RAnGbb_ZgslRY_bUc33_xVVLL3UJHrlL4QREW81-iZRl0130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP151867.RAnGbb_ZgslRY_bUc33_xVVLL3UJHrlL4QREW81-iZRl0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP151867.RAnGbb_ZgslRY_bUc33_xVVLL3UJHrlL4QREW81-iZRl0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP151867.RAnGbb_ZgslRY_bUc33_xVVLL3UJHrlL4QREW81-iZRl0130_provenance.
- NP151867.RAnGbb_ZgslRY_bUc33_xVVLL3UJHrlL4QREW81-iZRl0130_assertion description "[Carrier frequency of autosomal-recessive disorders in the Ashkenazi Jewish population: should the rationale for mutation choice for screening be reevaluated?]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP151867.RAnGbb_ZgslRY_bUc33_xVVLL3UJHrlL4QREW81-iZRl0130_provenance.
- NP151867.RAnGbb_ZgslRY_bUc33_xVVLL3UJHrlL4QREW81-iZRl0130_assertion evidence source_evidence_literature NP151867.RAnGbb_ZgslRY_bUc33_xVVLL3UJHrlL4QREW81-iZRl0130_provenance.
- NP151867.RAnGbb_ZgslRY_bUc33_xVVLL3UJHrlL4QREW81-iZRl0130_assertion SIO_000772 18264947 NP151867.RAnGbb_ZgslRY_bUc33_xVVLL3UJHrlL4QREW81-iZRl0130_provenance.
- NP151867.RAnGbb_ZgslRY_bUc33_xVVLL3UJHrlL4QREW81-iZRl0130_assertion wasDerivedFrom gad-20150221 NP151867.RAnGbb_ZgslRY_bUc33_xVVLL3UJHrlL4QREW81-iZRl0130_provenance.
- NP151867.RAnGbb_ZgslRY_bUc33_xVVLL3UJHrlL4QREW81-iZRl0130_assertion wasGeneratedBy ECO_0000203 NP151867.RAnGbb_ZgslRY_bUc33_xVVLL3UJHrlL4QREW81-iZRl0130_provenance.
- gad-20150221 importedOn "2015-02-21" NP151867.RAnGbb_ZgslRY_bUc33_xVVLL3UJHrlL4QREW81-iZRl0130_provenance.