Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP732450.RAjZIVF2d4nqsoKnJM6YAJd2dutR1fEqxWI2zq9ScQ48g130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP732450.RAjZIVF2d4nqsoKnJM6YAJd2dutR1fEqxWI2zq9ScQ48g130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP732450.RAjZIVF2d4nqsoKnJM6YAJd2dutR1fEqxWI2zq9ScQ48g130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP732450.RAjZIVF2d4nqsoKnJM6YAJd2dutR1fEqxWI2zq9ScQ48g130_provenance.
- NP732450.RAjZIVF2d4nqsoKnJM6YAJd2dutR1fEqxWI2zq9ScQ48g130_assertion description "[Penetrance of FMR1 premutation associated pathologies in fragile X syndrome families.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP732450.RAjZIVF2d4nqsoKnJM6YAJd2dutR1fEqxWI2zq9ScQ48g130_provenance.
- NP732450.RAjZIVF2d4nqsoKnJM6YAJd2dutR1fEqxWI2zq9ScQ48g130_assertion evidence source_evidence_literature NP732450.RAjZIVF2d4nqsoKnJM6YAJd2dutR1fEqxWI2zq9ScQ48g130_provenance.
- NP732450.RAjZIVF2d4nqsoKnJM6YAJd2dutR1fEqxWI2zq9ScQ48g130_assertion SIO_000772 19367323 NP732450.RAjZIVF2d4nqsoKnJM6YAJd2dutR1fEqxWI2zq9ScQ48g130_provenance.
- NP732450.RAjZIVF2d4nqsoKnJM6YAJd2dutR1fEqxWI2zq9ScQ48g130_assertion wasDerivedFrom befree-2016 NP732450.RAjZIVF2d4nqsoKnJM6YAJd2dutR1fEqxWI2zq9ScQ48g130_provenance.
- NP732450.RAjZIVF2d4nqsoKnJM6YAJd2dutR1fEqxWI2zq9ScQ48g130_assertion wasGeneratedBy ECO_0000203 NP732450.RAjZIVF2d4nqsoKnJM6YAJd2dutR1fEqxWI2zq9ScQ48g130_provenance.
- befree-2016 importedOn "2016-02-19" NP732450.RAjZIVF2d4nqsoKnJM6YAJd2dutR1fEqxWI2zq9ScQ48g130_provenance.