Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1002283.RAQINQEmBWjtcVLODlfVvBy9fit_8-WdAb-1Fw48Jm8Xw130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP1002283.RAQINQEmBWjtcVLODlfVvBy9fit_8-WdAb-1Fw48Jm8Xw130_assertion type Assertion NP1002283.RAQINQEmBWjtcVLODlfVvBy9fit_8-WdAb-1Fw48Jm8Xw130_head.
- NP1002283.RAQINQEmBWjtcVLODlfVvBy9fit_8-WdAb-1Fw48Jm8Xw130_assertion description "[The present family shows absent hypopigmentation in two patients of a white family with a deletion in the OA1 gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1002283.RAQINQEmBWjtcVLODlfVvBy9fit_8-WdAb-1Fw48Jm8Xw130_provenance.
- NP1002283.RAQINQEmBWjtcVLODlfVvBy9fit_8-WdAb-1Fw48Jm8Xw130_assertion evidence source_evidence_literature NP1002283.RAQINQEmBWjtcVLODlfVvBy9fit_8-WdAb-1Fw48Jm8Xw130_provenance.
- NP1002283.RAQINQEmBWjtcVLODlfVvBy9fit_8-WdAb-1Fw48Jm8Xw130_assertion SIO_000772 11520764 NP1002283.RAQINQEmBWjtcVLODlfVvBy9fit_8-WdAb-1Fw48Jm8Xw130_provenance.
- NP1002283.RAQINQEmBWjtcVLODlfVvBy9fit_8-WdAb-1Fw48Jm8Xw130_assertion wasDerivedFrom befree-20150227 NP1002283.RAQINQEmBWjtcVLODlfVvBy9fit_8-WdAb-1Fw48Jm8Xw130_provenance.
- NP1002283.RAQINQEmBWjtcVLODlfVvBy9fit_8-WdAb-1Fw48Jm8Xw130_assertion wasGeneratedBy ECO_0000203 NP1002283.RAQINQEmBWjtcVLODlfVvBy9fit_8-WdAb-1Fw48Jm8Xw130_provenance.