Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1344389.RAki-U9a97rU2N7vEurAptX9BRSVqqMfVOgCRmlizXU34130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1344389.RAki-U9a97rU2N7vEurAptX9BRSVqqMfVOgCRmlizXU34130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1344389.RAki-U9a97rU2N7vEurAptX9BRSVqqMfVOgCRmlizXU34130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1344389.RAki-U9a97rU2N7vEurAptX9BRSVqqMfVOgCRmlizXU34130_provenance.
- befree-2016 importedOn "2016-02-19" NP1344389.RAki-U9a97rU2N7vEurAptX9BRSVqqMfVOgCRmlizXU34130_provenance.
- NP1344389.RAki-U9a97rU2N7vEurAptX9BRSVqqMfVOgCRmlizXU34130_assertion wasGeneratedBy ECO_0000203 NP1344389.RAki-U9a97rU2N7vEurAptX9BRSVqqMfVOgCRmlizXU34130_provenance.
- NP1344389.RAki-U9a97rU2N7vEurAptX9BRSVqqMfVOgCRmlizXU34130_assertion wasDerivedFrom befree-2016 NP1344389.RAki-U9a97rU2N7vEurAptX9BRSVqqMfVOgCRmlizXU34130_provenance.
- NP1344389.RAki-U9a97rU2N7vEurAptX9BRSVqqMfVOgCRmlizXU34130_assertion SIO_000772 8530067 NP1344389.RAki-U9a97rU2N7vEurAptX9BRSVqqMfVOgCRmlizXU34130_provenance.
- NP1344389.RAki-U9a97rU2N7vEurAptX9BRSVqqMfVOgCRmlizXU34130_assertion evidence source_evidence_literature NP1344389.RAki-U9a97rU2N7vEurAptX9BRSVqqMfVOgCRmlizXU34130_provenance.
- NP1344389.RAki-U9a97rU2N7vEurAptX9BRSVqqMfVOgCRmlizXU34130_assertion description "[Two forms of inherited childhood nonsyndromic deafness (DFNB1 and DFNA3) and a Duchenne-like form of progressive muscular dystrophy (LGMD2C) have been mapped to the pericentromeric region of chromosome 13.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1344389.RAki-U9a97rU2N7vEurAptX9BRSVqqMfVOgCRmlizXU34130_provenance.