Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP237158.RAhY8kgWJRkNecibDrPyau2PI_ESPVau8ljv_MZvmEics130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP237158.RAhY8kgWJRkNecibDrPyau2PI_ESPVau8ljv_MZvmEics130_assertion type Assertion NP237158.RAhY8kgWJRkNecibDrPyau2PI_ESPVau8ljv_MZvmEics130_head.
- NP237158.RAhY8kgWJRkNecibDrPyau2PI_ESPVau8ljv_MZvmEics130_assertion wasGeneratedBy ECO_0000203 NP237158.RAhY8kgWJRkNecibDrPyau2PI_ESPVau8ljv_MZvmEics130_provenance.
- NP237158.RAhY8kgWJRkNecibDrPyau2PI_ESPVau8ljv_MZvmEics130_assertion wasDerivedFrom befree-20150227 NP237158.RAhY8kgWJRkNecibDrPyau2PI_ESPVau8ljv_MZvmEics130_provenance.
- NP237158.RAhY8kgWJRkNecibDrPyau2PI_ESPVau8ljv_MZvmEics130_assertion SIO_000772 20357205 NP237158.RAhY8kgWJRkNecibDrPyau2PI_ESPVau8ljv_MZvmEics130_provenance.
- NP237158.RAhY8kgWJRkNecibDrPyau2PI_ESPVau8ljv_MZvmEics130_assertion evidence source_evidence_literature NP237158.RAhY8kgWJRkNecibDrPyau2PI_ESPVau8ljv_MZvmEics130_provenance.
- NP237158.RAhY8kgWJRkNecibDrPyau2PI_ESPVau8ljv_MZvmEics130_assertion description "[Common mutations for Leber's hereditary optic neuropathy (LHON: G11778A; T14484C; and G3460A) were not present in AMD samples.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP237158.RAhY8kgWJRkNecibDrPyau2PI_ESPVau8ljv_MZvmEics130_provenance.