Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP985422.RAZiGdepMN1T8TSPe99xCHE0-L6tfbEgo91ATn_gR_kkU130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP985422.RAZiGdepMN1T8TSPe99xCHE0-L6tfbEgo91ATn_gR_kkU130_assertion type Assertion NP985422.RAZiGdepMN1T8TSPe99xCHE0-L6tfbEgo91ATn_gR_kkU130_head.
- NP985422.RAZiGdepMN1T8TSPe99xCHE0-L6tfbEgo91ATn_gR_kkU130_assertion wasGeneratedBy ECO_0000203 NP985422.RAZiGdepMN1T8TSPe99xCHE0-L6tfbEgo91ATn_gR_kkU130_provenance.
- NP985422.RAZiGdepMN1T8TSPe99xCHE0-L6tfbEgo91ATn_gR_kkU130_assertion wasDerivedFrom befree-20150227 NP985422.RAZiGdepMN1T8TSPe99xCHE0-L6tfbEgo91ATn_gR_kkU130_provenance.
- NP985422.RAZiGdepMN1T8TSPe99xCHE0-L6tfbEgo91ATn_gR_kkU130_assertion SIO_000772 21844578 NP985422.RAZiGdepMN1T8TSPe99xCHE0-L6tfbEgo91ATn_gR_kkU130_provenance.
- NP985422.RAZiGdepMN1T8TSPe99xCHE0-L6tfbEgo91ATn_gR_kkU130_assertion evidence source_evidence_literature NP985422.RAZiGdepMN1T8TSPe99xCHE0-L6tfbEgo91ATn_gR_kkU130_provenance.
- NP985422.RAZiGdepMN1T8TSPe99xCHE0-L6tfbEgo91ATn_gR_kkU130_assertion description "[Two novel PEX1 mutations in a patient with Zellweger syndrome: the first Korean case confirmed by biochemical, and molecular evidence.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP985422.RAZiGdepMN1T8TSPe99xCHE0-L6tfbEgo91ATn_gR_kkU130_provenance.