Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1242244.RANdyI468hLplRysc4vqBxc-oO9ha_APQ8lSi1RlMlRts130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1242244.RANdyI468hLplRysc4vqBxc-oO9ha_APQ8lSi1RlMlRts130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1242244.RANdyI468hLplRysc4vqBxc-oO9ha_APQ8lSi1RlMlRts130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1242244.RANdyI468hLplRysc4vqBxc-oO9ha_APQ8lSi1RlMlRts130_provenance.
- NP1242244.RANdyI468hLplRysc4vqBxc-oO9ha_APQ8lSi1RlMlRts130_assertion description "[Authors describe clinical, pathological, imaging and genetic findings in the first Irish family with Laing distal myopathy in whom a novel mutation in the human slow ?-myosin heavy chain (MYH7) gene has been identified.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1242244.RANdyI468hLplRysc4vqBxc-oO9ha_APQ8lSi1RlMlRts130_provenance.
- NP1242244.RANdyI468hLplRysc4vqBxc-oO9ha_APQ8lSi1RlMlRts130_assertion evidence source_evidence_literature NP1242244.RANdyI468hLplRysc4vqBxc-oO9ha_APQ8lSi1RlMlRts130_provenance.
- NP1242244.RANdyI468hLplRysc4vqBxc-oO9ha_APQ8lSi1RlMlRts130_assertion SIO_000772 25447691 NP1242244.RANdyI468hLplRysc4vqBxc-oO9ha_APQ8lSi1RlMlRts130_provenance.
- NP1242244.RANdyI468hLplRysc4vqBxc-oO9ha_APQ8lSi1RlMlRts130_assertion wasDerivedFrom befree-2016 NP1242244.RANdyI468hLplRysc4vqBxc-oO9ha_APQ8lSi1RlMlRts130_provenance.
- NP1242244.RANdyI468hLplRysc4vqBxc-oO9ha_APQ8lSi1RlMlRts130_assertion wasGeneratedBy ECO_0000203 NP1242244.RANdyI468hLplRysc4vqBxc-oO9ha_APQ8lSi1RlMlRts130_provenance.
- befree-2016 importedOn "2016-02-19" NP1242244.RANdyI468hLplRysc4vqBxc-oO9ha_APQ8lSi1RlMlRts130_provenance.