Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP664336.RADc7TPJsfcA1EW6CJl6DkPBOC6wve0xoxwMAvMw1c07Y130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP664336.RADc7TPJsfcA1EW6CJl6DkPBOC6wve0xoxwMAvMw1c07Y130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP664336.RADc7TPJsfcA1EW6CJl6DkPBOC6wve0xoxwMAvMw1c07Y130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP664336.RADc7TPJsfcA1EW6CJl6DkPBOC6wve0xoxwMAvMw1c07Y130_provenance.
- befree-2016 importedOn "2016-02-19" NP664336.RADc7TPJsfcA1EW6CJl6DkPBOC6wve0xoxwMAvMw1c07Y130_provenance.
- NP664336.RADc7TPJsfcA1EW6CJl6DkPBOC6wve0xoxwMAvMw1c07Y130_assertion wasGeneratedBy ECO_0000203 NP664336.RADc7TPJsfcA1EW6CJl6DkPBOC6wve0xoxwMAvMw1c07Y130_provenance.
- NP664336.RADc7TPJsfcA1EW6CJl6DkPBOC6wve0xoxwMAvMw1c07Y130_assertion wasDerivedFrom befree-2016 NP664336.RADc7TPJsfcA1EW6CJl6DkPBOC6wve0xoxwMAvMw1c07Y130_provenance.
- NP664336.RADc7TPJsfcA1EW6CJl6DkPBOC6wve0xoxwMAvMw1c07Y130_assertion SIO_000772 18392654 NP664336.RADc7TPJsfcA1EW6CJl6DkPBOC6wve0xoxwMAvMw1c07Y130_provenance.
- NP664336.RADc7TPJsfcA1EW6CJl6DkPBOC6wve0xoxwMAvMw1c07Y130_assertion evidence source_evidence_literature NP664336.RADc7TPJsfcA1EW6CJl6DkPBOC6wve0xoxwMAvMw1c07Y130_provenance.
- NP664336.RADc7TPJsfcA1EW6CJl6DkPBOC6wve0xoxwMAvMw1c07Y130_assertion description "[The differences between the nature of the human and mouse genomic abnormalities argue against models proposed so far that either envisioned SHFM3 as a local trisomy or Dac as a mutant allele of Fbxw4.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP664336.RADc7TPJsfcA1EW6CJl6DkPBOC6wve0xoxwMAvMw1c07Y130_provenance.