Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1294945.RAh9-7AtuVs1lKYZdm-rT2x7Dql21fLdBqtungtOjQg4U130_assertion> ?p ?o ?g. }
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- NP1294945.RAh9-7AtuVs1lKYZdm-rT2x7Dql21fLdBqtungtOjQg4U130_assertion type Assertion NP1294945.RAh9-7AtuVs1lKYZdm-rT2x7Dql21fLdBqtungtOjQg4U130_head.
- NP1294945.RAh9-7AtuVs1lKYZdm-rT2x7Dql21fLdBqtungtOjQg4U130_assertion description "[Interestingly, 50% of NS individuals with an NRAS mutation (including our family) present with lentigines and/or Caf�-au-lait spots.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1294945.RAh9-7AtuVs1lKYZdm-rT2x7Dql21fLdBqtungtOjQg4U130_provenance.
- NP1294945.RAh9-7AtuVs1lKYZdm-rT2x7Dql21fLdBqtungtOjQg4U130_assertion evidence source_evidence_literature NP1294945.RAh9-7AtuVs1lKYZdm-rT2x7Dql21fLdBqtungtOjQg4U130_provenance.
- NP1294945.RAh9-7AtuVs1lKYZdm-rT2x7Dql21fLdBqtungtOjQg4U130_assertion SIO_000772 26467218 NP1294945.RAh9-7AtuVs1lKYZdm-rT2x7Dql21fLdBqtungtOjQg4U130_provenance.
- NP1294945.RAh9-7AtuVs1lKYZdm-rT2x7Dql21fLdBqtungtOjQg4U130_assertion wasDerivedFrom befree-2016 NP1294945.RAh9-7AtuVs1lKYZdm-rT2x7Dql21fLdBqtungtOjQg4U130_provenance.
- NP1294945.RAh9-7AtuVs1lKYZdm-rT2x7Dql21fLdBqtungtOjQg4U130_assertion wasGeneratedBy ECO_0000203 NP1294945.RAh9-7AtuVs1lKYZdm-rT2x7Dql21fLdBqtungtOjQg4U130_provenance.