Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1030143.RAdcE-DpFks1yM72YEyei_HUNclLgfUs1aAAXxEF_LcXI130_assertion> ?p ?o ?g. }
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- NP1030143.RAdcE-DpFks1yM72YEyei_HUNclLgfUs1aAAXxEF_LcXI130_assertion type Assertion NP1030143.RAdcE-DpFks1yM72YEyei_HUNclLgfUs1aAAXxEF_LcXI130_head.
- NP1030143.RAdcE-DpFks1yM72YEyei_HUNclLgfUs1aAAXxEF_LcXI130_assertion wasGeneratedBy ECO_0000203 NP1030143.RAdcE-DpFks1yM72YEyei_HUNclLgfUs1aAAXxEF_LcXI130_provenance.
- NP1030143.RAdcE-DpFks1yM72YEyei_HUNclLgfUs1aAAXxEF_LcXI130_assertion wasDerivedFrom befree-2016 NP1030143.RAdcE-DpFks1yM72YEyei_HUNclLgfUs1aAAXxEF_LcXI130_provenance.
- NP1030143.RAdcE-DpFks1yM72YEyei_HUNclLgfUs1aAAXxEF_LcXI130_assertion SIO_000772 23171239 NP1030143.RAdcE-DpFks1yM72YEyei_HUNclLgfUs1aAAXxEF_LcXI130_provenance.
- NP1030143.RAdcE-DpFks1yM72YEyei_HUNclLgfUs1aAAXxEF_LcXI130_assertion evidence source_evidence_literature NP1030143.RAdcE-DpFks1yM72YEyei_HUNclLgfUs1aAAXxEF_LcXI130_provenance.
- NP1030143.RAdcE-DpFks1yM72YEyei_HUNclLgfUs1aAAXxEF_LcXI130_assertion description "[Oculocutaneous albinism type 4 (OCA4) is caused by autosomal recessive mutations in SLC45A2.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1030143.RAdcE-DpFks1yM72YEyei_HUNclLgfUs1aAAXxEF_LcXI130_provenance.