Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP674550.RA9yhRSMMK8PM7b9utnJHlrN1M5zofeM2GTQ9-yLeWAaA130_assertion> ?p ?o ?g. }
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- NP674550.RA9yhRSMMK8PM7b9utnJHlrN1M5zofeM2GTQ9-yLeWAaA130_assertion type Assertion NP674550.RA9yhRSMMK8PM7b9utnJHlrN1M5zofeM2GTQ9-yLeWAaA130_head.
- NP674550.RA9yhRSMMK8PM7b9utnJHlrN1M5zofeM2GTQ9-yLeWAaA130_assertion wasGeneratedBy ECO_0000203 NP674550.RA9yhRSMMK8PM7b9utnJHlrN1M5zofeM2GTQ9-yLeWAaA130_provenance.
- NP674550.RA9yhRSMMK8PM7b9utnJHlrN1M5zofeM2GTQ9-yLeWAaA130_assertion wasDerivedFrom befree-20150227 NP674550.RA9yhRSMMK8PM7b9utnJHlrN1M5zofeM2GTQ9-yLeWAaA130_provenance.
- NP674550.RA9yhRSMMK8PM7b9utnJHlrN1M5zofeM2GTQ9-yLeWAaA130_assertion SIO_000772 23372056 NP674550.RA9yhRSMMK8PM7b9utnJHlrN1M5zofeM2GTQ9-yLeWAaA130_provenance.
- NP674550.RA9yhRSMMK8PM7b9utnJHlrN1M5zofeM2GTQ9-yLeWAaA130_assertion evidence source_evidence_literature NP674550.RA9yhRSMMK8PM7b9utnJHlrN1M5zofeM2GTQ9-yLeWAaA130_provenance.
- NP674550.RA9yhRSMMK8PM7b9utnJHlrN1M5zofeM2GTQ9-yLeWAaA130_assertion description "[Direct sequencing of RPGR and RP2 allowed for identification of a disease-causing mutation in 21 families.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP674550.RA9yhRSMMK8PM7b9utnJHlrN1M5zofeM2GTQ9-yLeWAaA130_provenance.