Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP978022.RAsHWE1NfSkho1Hz4EAFdvTuO2WT91UCWj3tLluuHnPiw130_assertion> ?p ?o ?g. }
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- NP978022.RAsHWE1NfSkho1Hz4EAFdvTuO2WT91UCWj3tLluuHnPiw130_assertion type Assertion NP978022.RAsHWE1NfSkho1Hz4EAFdvTuO2WT91UCWj3tLluuHnPiw130_head.
- NP978022.RAsHWE1NfSkho1Hz4EAFdvTuO2WT91UCWj3tLluuHnPiw130_assertion description "[Novel KCNV2 mutations in cone dystrophy with supernormal rod electroretinogram.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP978022.RAsHWE1NfSkho1Hz4EAFdvTuO2WT91UCWj3tLluuHnPiw130_provenance.
- NP978022.RAsHWE1NfSkho1Hz4EAFdvTuO2WT91UCWj3tLluuHnPiw130_assertion evidence source_evidence_literature NP978022.RAsHWE1NfSkho1Hz4EAFdvTuO2WT91UCWj3tLluuHnPiw130_provenance.
- NP978022.RAsHWE1NfSkho1Hz4EAFdvTuO2WT91UCWj3tLluuHnPiw130_assertion SIO_000772 18400204 NP978022.RAsHWE1NfSkho1Hz4EAFdvTuO2WT91UCWj3tLluuHnPiw130_provenance.
- NP978022.RAsHWE1NfSkho1Hz4EAFdvTuO2WT91UCWj3tLluuHnPiw130_assertion wasDerivedFrom befree-20150227 NP978022.RAsHWE1NfSkho1Hz4EAFdvTuO2WT91UCWj3tLluuHnPiw130_provenance.
- NP978022.RAsHWE1NfSkho1Hz4EAFdvTuO2WT91UCWj3tLluuHnPiw130_assertion wasGeneratedBy ECO_0000203 NP978022.RAsHWE1NfSkho1Hz4EAFdvTuO2WT91UCWj3tLluuHnPiw130_provenance.