Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP701659.RAG8CRpnen2XnTzlRe-T5HQIAfGYsbt3ka-hn7dXp_aLA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP701659.RAG8CRpnen2XnTzlRe-T5HQIAfGYsbt3ka-hn7dXp_aLA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP701659.RAG8CRpnen2XnTzlRe-T5HQIAfGYsbt3ka-hn7dXp_aLA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP701659.RAG8CRpnen2XnTzlRe-T5HQIAfGYsbt3ka-hn7dXp_aLA130_provenance.
- NP701659.RAG8CRpnen2XnTzlRe-T5HQIAfGYsbt3ka-hn7dXp_aLA130_assertion description "[The five most prevalent diagnoses were Fanconi anemia (FA), Shwachman-Diamond syndrome (SDS), Diamond-Blackfan anemia (DBA), dyskeratosis congenita (DKC), and Kostmann's neutropenia (KS).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP701659.RAG8CRpnen2XnTzlRe-T5HQIAfGYsbt3ka-hn7dXp_aLA130_provenance.
- NP701659.RAG8CRpnen2XnTzlRe-T5HQIAfGYsbt3ka-hn7dXp_aLA130_assertion evidence source_evidence_literature NP701659.RAG8CRpnen2XnTzlRe-T5HQIAfGYsbt3ka-hn7dXp_aLA130_provenance.
- NP701659.RAG8CRpnen2XnTzlRe-T5HQIAfGYsbt3ka-hn7dXp_aLA130_assertion SIO_000772 16676307 NP701659.RAG8CRpnen2XnTzlRe-T5HQIAfGYsbt3ka-hn7dXp_aLA130_provenance.
- NP701659.RAG8CRpnen2XnTzlRe-T5HQIAfGYsbt3ka-hn7dXp_aLA130_assertion wasDerivedFrom befree-20140225 NP701659.RAG8CRpnen2XnTzlRe-T5HQIAfGYsbt3ka-hn7dXp_aLA130_provenance.
- NP701659.RAG8CRpnen2XnTzlRe-T5HQIAfGYsbt3ka-hn7dXp_aLA130_assertion wasGeneratedBy ECO_0000203 NP701659.RAG8CRpnen2XnTzlRe-T5HQIAfGYsbt3ka-hn7dXp_aLA130_provenance.
- befree-20140225 importedOn "2014-02-25" NP701659.RAG8CRpnen2XnTzlRe-T5HQIAfGYsbt3ka-hn7dXp_aLA130_provenance.