Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1030141.RAgg0eH-TybXTj-Pu30B41UL3SBlIban0_Xuypgs2Rj9c130_assertion> ?p ?o ?g. }
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- NP1030141.RAgg0eH-TybXTj-Pu30B41UL3SBlIban0_Xuypgs2Rj9c130_assertion type Assertion NP1030141.RAgg0eH-TybXTj-Pu30B41UL3SBlIban0_Xuypgs2Rj9c130_head.
- NP1030141.RAgg0eH-TybXTj-Pu30B41UL3SBlIban0_Xuypgs2Rj9c130_assertion wasGeneratedBy ECO_0000203 NP1030141.RAgg0eH-TybXTj-Pu30B41UL3SBlIban0_Xuypgs2Rj9c130_provenance.
- NP1030141.RAgg0eH-TybXTj-Pu30B41UL3SBlIban0_Xuypgs2Rj9c130_assertion wasDerivedFrom befree-2016 NP1030141.RAgg0eH-TybXTj-Pu30B41UL3SBlIban0_Xuypgs2Rj9c130_provenance.
- NP1030141.RAgg0eH-TybXTj-Pu30B41UL3SBlIban0_Xuypgs2Rj9c130_assertion SIO_000772 23171239 NP1030141.RAgg0eH-TybXTj-Pu30B41UL3SBlIban0_Xuypgs2Rj9c130_provenance.
- NP1030141.RAgg0eH-TybXTj-Pu30B41UL3SBlIban0_Xuypgs2Rj9c130_assertion evidence source_evidence_literature NP1030141.RAgg0eH-TybXTj-Pu30B41UL3SBlIban0_Xuypgs2Rj9c130_provenance.
- NP1030141.RAgg0eH-TybXTj-Pu30B41UL3SBlIban0_Xuypgs2Rj9c130_assertion description "[The sister also has a homozygous mutation in SLC45A2, which explains her severe oculocutaneous hypopigmentation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1030141.RAgg0eH-TybXTj-Pu30B41UL3SBlIban0_Xuypgs2Rj9c130_provenance.