Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP237795.RAa3dLyNQnzrcfm4nY5d16BN0BZ5FgawJWW5Ph9um998s130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP237795.RAa3dLyNQnzrcfm4nY5d16BN0BZ5FgawJWW5Ph9um998s130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP237795.RAa3dLyNQnzrcfm4nY5d16BN0BZ5FgawJWW5Ph9um998s130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP237795.RAa3dLyNQnzrcfm4nY5d16BN0BZ5FgawJWW5Ph9um998s130_provenance.
- NP237795.RAa3dLyNQnzrcfm4nY5d16BN0BZ5FgawJWW5Ph9um998s130_assertion description "[Mutations in the BIN1 gene cause centronuclear myopathy, which shares some histopathological features with myotonic dystrophy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP237795.RAa3dLyNQnzrcfm4nY5d16BN0BZ5FgawJWW5Ph9um998s130_provenance.
- NP237795.RAa3dLyNQnzrcfm4nY5d16BN0BZ5FgawJWW5Ph9um998s130_assertion evidence source_evidence_literature NP237795.RAa3dLyNQnzrcfm4nY5d16BN0BZ5FgawJWW5Ph9um998s130_provenance.
- NP237795.RAa3dLyNQnzrcfm4nY5d16BN0BZ5FgawJWW5Ph9um998s130_assertion SIO_000772 21623381 NP237795.RAa3dLyNQnzrcfm4nY5d16BN0BZ5FgawJWW5Ph9um998s130_provenance.
- NP237795.RAa3dLyNQnzrcfm4nY5d16BN0BZ5FgawJWW5Ph9um998s130_assertion wasDerivedFrom befree-20150227 NP237795.RAa3dLyNQnzrcfm4nY5d16BN0BZ5FgawJWW5Ph9um998s130_provenance.
- NP237795.RAa3dLyNQnzrcfm4nY5d16BN0BZ5FgawJWW5Ph9um998s130_assertion wasGeneratedBy ECO_0000203 NP237795.RAa3dLyNQnzrcfm4nY5d16BN0BZ5FgawJWW5Ph9um998s130_provenance.
- befree-20150227 importedOn "2015-02-27" NP237795.RAa3dLyNQnzrcfm4nY5d16BN0BZ5FgawJWW5Ph9um998s130_provenance.