Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP520627.RAh8Fzx-EHB_1ZAdG4Es_43R0WXLARjnbeGimExWVQPz8130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP520627.RAh8Fzx-EHB_1ZAdG4Es_43R0WXLARjnbeGimExWVQPz8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP520627.RAh8Fzx-EHB_1ZAdG4Es_43R0WXLARjnbeGimExWVQPz8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP520627.RAh8Fzx-EHB_1ZAdG4Es_43R0WXLARjnbeGimExWVQPz8130_provenance.
- NP520627.RAh8Fzx-EHB_1ZAdG4Es_43R0WXLARjnbeGimExWVQPz8130_assertion description "[In 5 patients with MEN 2A, gene rearrangements, such as a gross deletion, were not found in the 880 kb NruI fragment which covered the closest region to the MEN-2A locus from the RBP3 and D10S15 loci.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP520627.RAh8Fzx-EHB_1ZAdG4Es_43R0WXLARjnbeGimExWVQPz8130_provenance.
- NP520627.RAh8Fzx-EHB_1ZAdG4Es_43R0WXLARjnbeGimExWVQPz8130_assertion evidence source_evidence_literature NP520627.RAh8Fzx-EHB_1ZAdG4Es_43R0WXLARjnbeGimExWVQPz8130_provenance.
- NP520627.RAh8Fzx-EHB_1ZAdG4Es_43R0WXLARjnbeGimExWVQPz8130_assertion SIO_000772 1982737 NP520627.RAh8Fzx-EHB_1ZAdG4Es_43R0WXLARjnbeGimExWVQPz8130_provenance.
- NP520627.RAh8Fzx-EHB_1ZAdG4Es_43R0WXLARjnbeGimExWVQPz8130_assertion wasDerivedFrom befree-20140225 NP520627.RAh8Fzx-EHB_1ZAdG4Es_43R0WXLARjnbeGimExWVQPz8130_provenance.
- NP520627.RAh8Fzx-EHB_1ZAdG4Es_43R0WXLARjnbeGimExWVQPz8130_assertion wasGeneratedBy ECO_0000203 NP520627.RAh8Fzx-EHB_1ZAdG4Es_43R0WXLARjnbeGimExWVQPz8130_provenance.
- befree-20140225 importedOn "2014-02-25" NP520627.RAh8Fzx-EHB_1ZAdG4Es_43R0WXLARjnbeGimExWVQPz8130_provenance.