Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1410092.RAA6yd_HupqyRKgO1mwk_xWl9CnTYIBeVkq8Gvb4FAtZs130_assertion> ?p ?o ?g. }
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- NP1410092.RAA6yd_HupqyRKgO1mwk_xWl9CnTYIBeVkq8Gvb4FAtZs130_assertion type Assertion NP1410092.RAA6yd_HupqyRKgO1mwk_xWl9CnTYIBeVkq8Gvb4FAtZs130_head.
- NP1410092.RAA6yd_HupqyRKgO1mwk_xWl9CnTYIBeVkq8Gvb4FAtZs130_assertion description "[These results demonstrate that mutation in PEX16 is the genetic cause of CG-D PBDs.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1410092.RAA6yd_HupqyRKgO1mwk_xWl9CnTYIBeVkq8Gvb4FAtZs130_provenance.
- NP1410092.RAA6yd_HupqyRKgO1mwk_xWl9CnTYIBeVkq8Gvb4FAtZs130_assertion evidence source_evidence_literature NP1410092.RAA6yd_HupqyRKgO1mwk_xWl9CnTYIBeVkq8Gvb4FAtZs130_provenance.
- NP1410092.RAA6yd_HupqyRKgO1mwk_xWl9CnTYIBeVkq8Gvb4FAtZs130_assertion SIO_000772 9837814 NP1410092.RAA6yd_HupqyRKgO1mwk_xWl9CnTYIBeVkq8Gvb4FAtZs130_provenance.
- NP1410092.RAA6yd_HupqyRKgO1mwk_xWl9CnTYIBeVkq8Gvb4FAtZs130_assertion wasDerivedFrom befree-2016 NP1410092.RAA6yd_HupqyRKgO1mwk_xWl9CnTYIBeVkq8Gvb4FAtZs130_provenance.
- NP1410092.RAA6yd_HupqyRKgO1mwk_xWl9CnTYIBeVkq8Gvb4FAtZs130_assertion wasGeneratedBy ECO_0000203 NP1410092.RAA6yd_HupqyRKgO1mwk_xWl9CnTYIBeVkq8Gvb4FAtZs130_provenance.