Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP412837.RAoYhWMRfbCfy7QpFFs-s-1vvyNtNDEUR9lrLxC2r1JUQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP412837.RAoYhWMRfbCfy7QpFFs-s-1vvyNtNDEUR9lrLxC2r1JUQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP412837.RAoYhWMRfbCfy7QpFFs-s-1vvyNtNDEUR9lrLxC2r1JUQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP412837.RAoYhWMRfbCfy7QpFFs-s-1vvyNtNDEUR9lrLxC2r1JUQ130_provenance.
- NP412837.RAoYhWMRfbCfy7QpFFs-s-1vvyNtNDEUR9lrLxC2r1JUQ130_assertion description "[Elements of FMR2 were initially identified from sequences deleted from a developmentally delayed boy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP412837.RAoYhWMRfbCfy7QpFFs-s-1vvyNtNDEUR9lrLxC2r1JUQ130_provenance.
- NP412837.RAoYhWMRfbCfy7QpFFs-s-1vvyNtNDEUR9lrLxC2r1JUQ130_assertion evidence source_evidence_literature NP412837.RAoYhWMRfbCfy7QpFFs-s-1vvyNtNDEUR9lrLxC2r1JUQ130_provenance.
- NP412837.RAoYhWMRfbCfy7QpFFs-s-1vvyNtNDEUR9lrLxC2r1JUQ130_assertion SIO_000772 8673085 NP412837.RAoYhWMRfbCfy7QpFFs-s-1vvyNtNDEUR9lrLxC2r1JUQ130_provenance.
- NP412837.RAoYhWMRfbCfy7QpFFs-s-1vvyNtNDEUR9lrLxC2r1JUQ130_assertion wasDerivedFrom befree-20150227 NP412837.RAoYhWMRfbCfy7QpFFs-s-1vvyNtNDEUR9lrLxC2r1JUQ130_provenance.
- NP412837.RAoYhWMRfbCfy7QpFFs-s-1vvyNtNDEUR9lrLxC2r1JUQ130_assertion wasGeneratedBy ECO_0000203 NP412837.RAoYhWMRfbCfy7QpFFs-s-1vvyNtNDEUR9lrLxC2r1JUQ130_provenance.
- befree-20150227 importedOn "2015-02-27" NP412837.RAoYhWMRfbCfy7QpFFs-s-1vvyNtNDEUR9lrLxC2r1JUQ130_provenance.