Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1357905.RAOwBiVk3cAU5WR_UDERvv0sqrW8V5cgLoMKHxZQVgIxQ130_assertion> ?p ?o ?g. }
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- NP1357905.RAOwBiVk3cAU5WR_UDERvv0sqrW8V5cgLoMKHxZQVgIxQ130_assertion type Assertion NP1357905.RAOwBiVk3cAU5WR_UDERvv0sqrW8V5cgLoMKHxZQVgIxQ130_head.
- NP1357905.RAOwBiVk3cAU5WR_UDERvv0sqrW8V5cgLoMKHxZQVgIxQ130_assertion description "[We have identified six different point mutations in the HCS gene in nine patients with MCD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1357905.RAOwBiVk3cAU5WR_UDERvv0sqrW8V5cgLoMKHxZQVgIxQ130_provenance.
- NP1357905.RAOwBiVk3cAU5WR_UDERvv0sqrW8V5cgLoMKHxZQVgIxQ130_assertion evidence source_evidence_literature NP1357905.RAOwBiVk3cAU5WR_UDERvv0sqrW8V5cgLoMKHxZQVgIxQ130_provenance.
- NP1357905.RAOwBiVk3cAU5WR_UDERvv0sqrW8V5cgLoMKHxZQVgIxQ130_assertion SIO_000772 8817339 NP1357905.RAOwBiVk3cAU5WR_UDERvv0sqrW8V5cgLoMKHxZQVgIxQ130_provenance.
- NP1357905.RAOwBiVk3cAU5WR_UDERvv0sqrW8V5cgLoMKHxZQVgIxQ130_assertion wasDerivedFrom befree-2016 NP1357905.RAOwBiVk3cAU5WR_UDERvv0sqrW8V5cgLoMKHxZQVgIxQ130_provenance.
- NP1357905.RAOwBiVk3cAU5WR_UDERvv0sqrW8V5cgLoMKHxZQVgIxQ130_assertion wasGeneratedBy ECO_0000203 NP1357905.RAOwBiVk3cAU5WR_UDERvv0sqrW8V5cgLoMKHxZQVgIxQ130_provenance.