Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1175817.RAH75yvpba4U0B34UJdPpUUPPQQBemjZNGY8KJ2WhWnkU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1175817.RAH75yvpba4U0B34UJdPpUUPPQQBemjZNGY8KJ2WhWnkU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1175817.RAH75yvpba4U0B34UJdPpUUPPQQBemjZNGY8KJ2WhWnkU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1175817.RAH75yvpba4U0B34UJdPpUUPPQQBemjZNGY8KJ2WhWnkU130_provenance.
- NP1175817.RAH75yvpba4U0B34UJdPpUUPPQQBemjZNGY8KJ2WhWnkU130_assertion description "[It overlaps with Desbuquois dysplasia, Larsen syndrome and spondyloepiphyseal dysplasia with dislocations ascribed to CANT1, FLNB and CHST3 mutations, respectively.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1175817.RAH75yvpba4U0B34UJdPpUUPPQQBemjZNGY8KJ2WhWnkU130_provenance.
- NP1175817.RAH75yvpba4U0B34UJdPpUUPPQQBemjZNGY8KJ2WhWnkU130_assertion evidence source_evidence_literature NP1175817.RAH75yvpba4U0B34UJdPpUUPPQQBemjZNGY8KJ2WhWnkU130_provenance.
- NP1175817.RAH75yvpba4U0B34UJdPpUUPPQQBemjZNGY8KJ2WhWnkU130_assertion SIO_000772 24755949 NP1175817.RAH75yvpba4U0B34UJdPpUUPPQQBemjZNGY8KJ2WhWnkU130_provenance.
- NP1175817.RAH75yvpba4U0B34UJdPpUUPPQQBemjZNGY8KJ2WhWnkU130_assertion wasDerivedFrom befree-2016 NP1175817.RAH75yvpba4U0B34UJdPpUUPPQQBemjZNGY8KJ2WhWnkU130_provenance.
- NP1175817.RAH75yvpba4U0B34UJdPpUUPPQQBemjZNGY8KJ2WhWnkU130_assertion wasGeneratedBy ECO_0000203 NP1175817.RAH75yvpba4U0B34UJdPpUUPPQQBemjZNGY8KJ2WhWnkU130_provenance.
- befree-2016 importedOn "2016-02-19" NP1175817.RAH75yvpba4U0B34UJdPpUUPPQQBemjZNGY8KJ2WhWnkU130_provenance.