Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP1720.RA_4eWrolK2Ifnk95ipLRlzK0O9EWFDvzeRVZJWnUTMb0130_assertion> ?p ?o ?g. }
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- NP1720.RA_4eWrolK2Ifnk95ipLRlzK0O9EWFDvzeRVZJWnUTMb0130_assertion type Assertion NP1720.RA_4eWrolK2Ifnk95ipLRlzK0O9EWFDvzeRVZJWnUTMb0130_head.
- NP1720.RA_4eWrolK2Ifnk95ipLRlzK0O9EWFDvzeRVZJWnUTMb0130_assertion description "[The BCD region of chromosome 4q35.1 was refined to an interval flanked centromerically by D4S2924 by linkage and haplotype analysis; mutations were found in the novel CYP450 family member CYP4V2 in 23 of 25 unrelated patients with BCD tested.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1720.RA_4eWrolK2Ifnk95ipLRlzK0O9EWFDvzeRVZJWnUTMb0130_provenance.
- NP1720.RA_4eWrolK2Ifnk95ipLRlzK0O9EWFDvzeRVZJWnUTMb0130_assertion evidence source_evidence_curated NP1720.RA_4eWrolK2Ifnk95ipLRlzK0O9EWFDvzeRVZJWnUTMb0130_provenance.
- NP1720.RA_4eWrolK2Ifnk95ipLRlzK0O9EWFDvzeRVZJWnUTMb0130_assertion SIO_000772 15042513 NP1720.RA_4eWrolK2Ifnk95ipLRlzK0O9EWFDvzeRVZJWnUTMb0130_provenance.
- NP1720.RA_4eWrolK2Ifnk95ipLRlzK0O9EWFDvzeRVZJWnUTMb0130_assertion wasDerivedFrom uniprot-20130724 NP1720.RA_4eWrolK2Ifnk95ipLRlzK0O9EWFDvzeRVZJWnUTMb0130_provenance.
- NP1720.RA_4eWrolK2Ifnk95ipLRlzK0O9EWFDvzeRVZJWnUTMb0130_assertion wasGeneratedBy ECO_0000218 NP1720.RA_4eWrolK2Ifnk95ipLRlzK0O9EWFDvzeRVZJWnUTMb0130_provenance.