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- NP1410093.RAkMD8VeF67lVIiJOBYHKMsTPcz1fdBMqQBZ1POBgQClU130_assertion type Assertion NP1410093.RAkMD8VeF67lVIiJOBYHKMsTPcz1fdBMqQBZ1POBgQClU130_head.
- NP1410093.RAkMD8VeF67lVIiJOBYHKMsTPcz1fdBMqQBZ1POBgQClU130_assertion description "[Mutation in PEX16 is causal in the peroxisome-deficient Zellweger syndrome of complementation group D.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1410093.RAkMD8VeF67lVIiJOBYHKMsTPcz1fdBMqQBZ1POBgQClU130_provenance.
- NP1410093.RAkMD8VeF67lVIiJOBYHKMsTPcz1fdBMqQBZ1POBgQClU130_assertion evidence source_evidence_literature NP1410093.RAkMD8VeF67lVIiJOBYHKMsTPcz1fdBMqQBZ1POBgQClU130_provenance.
- NP1410093.RAkMD8VeF67lVIiJOBYHKMsTPcz1fdBMqQBZ1POBgQClU130_assertion SIO_000772 9837814 NP1410093.RAkMD8VeF67lVIiJOBYHKMsTPcz1fdBMqQBZ1POBgQClU130_provenance.
- NP1410093.RAkMD8VeF67lVIiJOBYHKMsTPcz1fdBMqQBZ1POBgQClU130_assertion wasDerivedFrom befree-2016 NP1410093.RAkMD8VeF67lVIiJOBYHKMsTPcz1fdBMqQBZ1POBgQClU130_provenance.
- NP1410093.RAkMD8VeF67lVIiJOBYHKMsTPcz1fdBMqQBZ1POBgQClU130_assertion wasGeneratedBy ECO_0000203 NP1410093.RAkMD8VeF67lVIiJOBYHKMsTPcz1fdBMqQBZ1POBgQClU130_provenance.