Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP929190.RAnXJ3x5AJzjgBJnp9RXnr7Hze6WnXNvAb6bt1vZw9mxQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP929190.RAnXJ3x5AJzjgBJnp9RXnr7Hze6WnXNvAb6bt1vZw9mxQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP929190.RAnXJ3x5AJzjgBJnp9RXnr7Hze6WnXNvAb6bt1vZw9mxQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP929190.RAnXJ3x5AJzjgBJnp9RXnr7Hze6WnXNvAb6bt1vZw9mxQ130_provenance.
- NP929190.RAnXJ3x5AJzjgBJnp9RXnr7Hze6WnXNvAb6bt1vZw9mxQ130_assertion wasGeneratedBy ECO_0000203 NP929190.RAnXJ3x5AJzjgBJnp9RXnr7Hze6WnXNvAb6bt1vZw9mxQ130_provenance.
- NP929190.RAnXJ3x5AJzjgBJnp9RXnr7Hze6WnXNvAb6bt1vZw9mxQ130_assertion wasDerivedFrom befree-20140225 NP929190.RAnXJ3x5AJzjgBJnp9RXnr7Hze6WnXNvAb6bt1vZw9mxQ130_provenance.
- NP929190.RAnXJ3x5AJzjgBJnp9RXnr7Hze6WnXNvAb6bt1vZw9mxQ130_assertion SIO_000772 17097056 NP929190.RAnXJ3x5AJzjgBJnp9RXnr7Hze6WnXNvAb6bt1vZw9mxQ130_provenance.
- NP929190.RAnXJ3x5AJzjgBJnp9RXnr7Hze6WnXNvAb6bt1vZw9mxQ130_assertion evidence source_evidence_literature NP929190.RAnXJ3x5AJzjgBJnp9RXnr7Hze6WnXNvAb6bt1vZw9mxQ130_provenance.
- NP929190.RAnXJ3x5AJzjgBJnp9RXnr7Hze6WnXNvAb6bt1vZw9mxQ130_assertion description "[Thirteen of the 239 patients (5.4%) had one of 13 distinct HCM-associated Z-disc mutations involving residues highly conserved across species and absent in 600 reference alleles: LDB3 (6), ACTN2 (3), TCAP (1), CSRP3 (1), and VCL (2).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP929190.RAnXJ3x5AJzjgBJnp9RXnr7Hze6WnXNvAb6bt1vZw9mxQ130_provenance.
- befree-20140225 importedOn "2014-02-25" NP929190.RAnXJ3x5AJzjgBJnp9RXnr7Hze6WnXNvAb6bt1vZw9mxQ130_provenance.