Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP835908.RAsmWGC0wCpwm-jQT64l8PFEK0LCc8M2T-DM2np1T46X0130_assertion> ?p ?o ?g. }
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- NP835908.RAsmWGC0wCpwm-jQT64l8PFEK0LCc8M2T-DM2np1T46X0130_assertion type Assertion NP835908.RAsmWGC0wCpwm-jQT64l8PFEK0LCc8M2T-DM2np1T46X0130_head.
- NP835908.RAsmWGC0wCpwm-jQT64l8PFEK0LCc8M2T-DM2np1T46X0130_assertion description "[Mutations in ABCB6 cause dyschromatosis universalis hereditaria.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP835908.RAsmWGC0wCpwm-jQT64l8PFEK0LCc8M2T-DM2np1T46X0130_provenance.
- NP835908.RAsmWGC0wCpwm-jQT64l8PFEK0LCc8M2T-DM2np1T46X0130_assertion evidence source_evidence_literature NP835908.RAsmWGC0wCpwm-jQT64l8PFEK0LCc8M2T-DM2np1T46X0130_provenance.
- NP835908.RAsmWGC0wCpwm-jQT64l8PFEK0LCc8M2T-DM2np1T46X0130_assertion SIO_000772 23519333 NP835908.RAsmWGC0wCpwm-jQT64l8PFEK0LCc8M2T-DM2np1T46X0130_provenance.
- NP835908.RAsmWGC0wCpwm-jQT64l8PFEK0LCc8M2T-DM2np1T46X0130_assertion wasDerivedFrom befree-20150227 NP835908.RAsmWGC0wCpwm-jQT64l8PFEK0LCc8M2T-DM2np1T46X0130_provenance.
- NP835908.RAsmWGC0wCpwm-jQT64l8PFEK0LCc8M2T-DM2np1T46X0130_assertion wasGeneratedBy ECO_0000203 NP835908.RAsmWGC0wCpwm-jQT64l8PFEK0LCc8M2T-DM2np1T46X0130_provenance.