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- source_evidence_literature type ECO_0000212 NP538849.RAeKhCCln0bBtmUJ5ADldaBlt-K0l1su9bh9aXPE-pD1k130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP538849.RAeKhCCln0bBtmUJ5ADldaBlt-K0l1su9bh9aXPE-pD1k130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP538849.RAeKhCCln0bBtmUJ5ADldaBlt-K0l1su9bh9aXPE-pD1k130_provenance.
- NP538849.RAeKhCCln0bBtmUJ5ADldaBlt-K0l1su9bh9aXPE-pD1k130_assertion description "[(AC)n microsatellite polymorphism and 14-nucleotide deletion in exon 42 ankyrin-1 gene in several families with hereditary spherocytosis in a population of South-Western Poland.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP538849.RAeKhCCln0bBtmUJ5ADldaBlt-K0l1su9bh9aXPE-pD1k130_provenance.
- NP538849.RAeKhCCln0bBtmUJ5ADldaBlt-K0l1su9bh9aXPE-pD1k130_assertion evidence source_evidence_literature NP538849.RAeKhCCln0bBtmUJ5ADldaBlt-K0l1su9bh9aXPE-pD1k130_provenance.
- NP538849.RAeKhCCln0bBtmUJ5ADldaBlt-K0l1su9bh9aXPE-pD1k130_assertion SIO_000772 16518602 NP538849.RAeKhCCln0bBtmUJ5ADldaBlt-K0l1su9bh9aXPE-pD1k130_provenance.
- NP538849.RAeKhCCln0bBtmUJ5ADldaBlt-K0l1su9bh9aXPE-pD1k130_assertion wasDerivedFrom befree-2016 NP538849.RAeKhCCln0bBtmUJ5ADldaBlt-K0l1su9bh9aXPE-pD1k130_provenance.
- NP538849.RAeKhCCln0bBtmUJ5ADldaBlt-K0l1su9bh9aXPE-pD1k130_assertion wasGeneratedBy ECO_0000203 NP538849.RAeKhCCln0bBtmUJ5ADldaBlt-K0l1su9bh9aXPE-pD1k130_provenance.
- befree-2016 importedOn "2016-02-19" NP538849.RAeKhCCln0bBtmUJ5ADldaBlt-K0l1su9bh9aXPE-pD1k130_provenance.