Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP884487.RAOMPKGd9_HVnzznx_QuPNLd-8eqy_s1jgq4320o2-4jI130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP884487.RAOMPKGd9_HVnzznx_QuPNLd-8eqy_s1jgq4320o2-4jI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP884487.RAOMPKGd9_HVnzznx_QuPNLd-8eqy_s1jgq4320o2-4jI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP884487.RAOMPKGd9_HVnzznx_QuPNLd-8eqy_s1jgq4320o2-4jI130_provenance.
- NP884487.RAOMPKGd9_HVnzznx_QuPNLd-8eqy_s1jgq4320o2-4jI130_assertion description "[These findings demonstrate that heterozygous mutations toward the 3' end of MYH7 cause Laing-type early-onset distal myopathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP884487.RAOMPKGd9_HVnzznx_QuPNLd-8eqy_s1jgq4320o2-4jI130_provenance.
- NP884487.RAOMPKGd9_HVnzznx_QuPNLd-8eqy_s1jgq4320o2-4jI130_assertion evidence source_evidence_literature NP884487.RAOMPKGd9_HVnzznx_QuPNLd-8eqy_s1jgq4320o2-4jI130_provenance.
- NP884487.RAOMPKGd9_HVnzznx_QuPNLd-8eqy_s1jgq4320o2-4jI130_assertion SIO_000772 15322983 NP884487.RAOMPKGd9_HVnzznx_QuPNLd-8eqy_s1jgq4320o2-4jI130_provenance.
- NP884487.RAOMPKGd9_HVnzznx_QuPNLd-8eqy_s1jgq4320o2-4jI130_assertion wasDerivedFrom befree-20140225 NP884487.RAOMPKGd9_HVnzznx_QuPNLd-8eqy_s1jgq4320o2-4jI130_provenance.
- NP884487.RAOMPKGd9_HVnzznx_QuPNLd-8eqy_s1jgq4320o2-4jI130_assertion wasGeneratedBy ECO_0000203 NP884487.RAOMPKGd9_HVnzznx_QuPNLd-8eqy_s1jgq4320o2-4jI130_provenance.
- befree-20140225 importedOn "2014-02-25" NP884487.RAOMPKGd9_HVnzznx_QuPNLd-8eqy_s1jgq4320o2-4jI130_provenance.