Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP629603.RAFruDvEafjqZ9tmn91WzCuEQqLMnFGGK_0A7hr303bUQ130_assertion> ?p ?o ?g. }
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- NP629603.RAFruDvEafjqZ9tmn91WzCuEQqLMnFGGK_0A7hr303bUQ130_assertion type Assertion NP629603.RAFruDvEafjqZ9tmn91WzCuEQqLMnFGGK_0A7hr303bUQ130_head.
- NP629603.RAFruDvEafjqZ9tmn91WzCuEQqLMnFGGK_0A7hr303bUQ130_assertion description "[Cytogenetically invisible microdeletions involving PITX2 in Rieger syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP629603.RAFruDvEafjqZ9tmn91WzCuEQqLMnFGGK_0A7hr303bUQ130_provenance.
- NP629603.RAFruDvEafjqZ9tmn91WzCuEQqLMnFGGK_0A7hr303bUQ130_assertion evidence source_evidence_literature NP629603.RAFruDvEafjqZ9tmn91WzCuEQqLMnFGGK_0A7hr303bUQ130_provenance.
- NP629603.RAFruDvEafjqZ9tmn91WzCuEQqLMnFGGK_0A7hr303bUQ130_assertion SIO_000772 17850355 NP629603.RAFruDvEafjqZ9tmn91WzCuEQqLMnFGGK_0A7hr303bUQ130_provenance.
- NP629603.RAFruDvEafjqZ9tmn91WzCuEQqLMnFGGK_0A7hr303bUQ130_assertion wasDerivedFrom befree-2016 NP629603.RAFruDvEafjqZ9tmn91WzCuEQqLMnFGGK_0A7hr303bUQ130_provenance.
- NP629603.RAFruDvEafjqZ9tmn91WzCuEQqLMnFGGK_0A7hr303bUQ130_assertion wasGeneratedBy ECO_0000203 NP629603.RAFruDvEafjqZ9tmn91WzCuEQqLMnFGGK_0A7hr303bUQ130_provenance.