Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP741278.RA--yUOc6cYiL_tVVa9c4XIQTJ3sJ59ZgxRc-dGMTBC_g130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP741278.RA--yUOc6cYiL_tVVa9c4XIQTJ3sJ59ZgxRc-dGMTBC_g130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP741278.RA--yUOc6cYiL_tVVa9c4XIQTJ3sJ59ZgxRc-dGMTBC_g130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP741278.RA--yUOc6cYiL_tVVa9c4XIQTJ3sJ59ZgxRc-dGMTBC_g130_provenance.
- befree-2016 importedOn "2016-02-19" NP741278.RA--yUOc6cYiL_tVVa9c4XIQTJ3sJ59ZgxRc-dGMTBC_g130_provenance.
- NP741278.RA--yUOc6cYiL_tVVa9c4XIQTJ3sJ59ZgxRc-dGMTBC_g130_assertion wasGeneratedBy ECO_0000203 NP741278.RA--yUOc6cYiL_tVVa9c4XIQTJ3sJ59ZgxRc-dGMTBC_g130_provenance.
- NP741278.RA--yUOc6cYiL_tVVa9c4XIQTJ3sJ59ZgxRc-dGMTBC_g130_assertion wasDerivedFrom befree-2016 NP741278.RA--yUOc6cYiL_tVVa9c4XIQTJ3sJ59ZgxRc-dGMTBC_g130_provenance.
- NP741278.RA--yUOc6cYiL_tVVa9c4XIQTJ3sJ59ZgxRc-dGMTBC_g130_assertion SIO_000772 19473076 NP741278.RA--yUOc6cYiL_tVVa9c4XIQTJ3sJ59ZgxRc-dGMTBC_g130_provenance.
- NP741278.RA--yUOc6cYiL_tVVa9c4XIQTJ3sJ59ZgxRc-dGMTBC_g130_assertion evidence source_evidence_literature NP741278.RA--yUOc6cYiL_tVVa9c4XIQTJ3sJ59ZgxRc-dGMTBC_g130_provenance.
- NP741278.RA--yUOc6cYiL_tVVa9c4XIQTJ3sJ59ZgxRc-dGMTBC_g130_assertion description "[A novel mutation (C1425Y) in the FBN2 gene in a father and son with congenital contractural arachnodactyly.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP741278.RA--yUOc6cYiL_tVVa9c4XIQTJ3sJ59ZgxRc-dGMTBC_g130_provenance.