Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP66682.RAJAvd_sFwnweRVkbBT0CrSnCbflllqxAuBlhfP-so2n0130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP66682.RAJAvd_sFwnweRVkbBT0CrSnCbflllqxAuBlhfP-so2n0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP66682.RAJAvd_sFwnweRVkbBT0CrSnCbflllqxAuBlhfP-so2n0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP66682.RAJAvd_sFwnweRVkbBT0CrSnCbflllqxAuBlhfP-so2n0130_provenance.
- NP66682.RAJAvd_sFwnweRVkbBT0CrSnCbflllqxAuBlhfP-so2n0130_assertion description "[Highly penetrant, non-synonymous, or insertion-deletion mutations in TERF1 and TERF2 were not identified and therefore are not likely to be major genetic risk factors for the development of AA.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP66682.RAJAvd_sFwnweRVkbBT0CrSnCbflllqxAuBlhfP-so2n0130_provenance.
- NP66682.RAJAvd_sFwnweRVkbBT0CrSnCbflllqxAuBlhfP-so2n0130_assertion evidence source_evidence_literature NP66682.RAJAvd_sFwnweRVkbBT0CrSnCbflllqxAuBlhfP-so2n0130_provenance.
- NP66682.RAJAvd_sFwnweRVkbBT0CrSnCbflllqxAuBlhfP-so2n0130_assertion SIO_000772 16647572 NP66682.RAJAvd_sFwnweRVkbBT0CrSnCbflllqxAuBlhfP-so2n0130_provenance.
- NP66682.RAJAvd_sFwnweRVkbBT0CrSnCbflllqxAuBlhfP-so2n0130_assertion wasDerivedFrom gad-20130706 NP66682.RAJAvd_sFwnweRVkbBT0CrSnCbflllqxAuBlhfP-so2n0130_provenance.
- NP66682.RAJAvd_sFwnweRVkbBT0CrSnCbflllqxAuBlhfP-so2n0130_assertion wasGeneratedBy ECO_0000203 NP66682.RAJAvd_sFwnweRVkbBT0CrSnCbflllqxAuBlhfP-so2n0130_provenance.
- gad-20130706 importedOn "2013-07-06" NP66682.RAJAvd_sFwnweRVkbBT0CrSnCbflllqxAuBlhfP-so2n0130_provenance.