Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP606032.RA0_cQkdYe-gRo1a8jrYcYtdMqfmHdJ7OBxOLbHbWw10s130_assertion> ?p ?o ?g. }
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- NP606032.RA0_cQkdYe-gRo1a8jrYcYtdMqfmHdJ7OBxOLbHbWw10s130_assertion type Assertion NP606032.RA0_cQkdYe-gRo1a8jrYcYtdMqfmHdJ7OBxOLbHbWw10s130_head.
- NP606032.RA0_cQkdYe-gRo1a8jrYcYtdMqfmHdJ7OBxOLbHbWw10s130_assertion description "[Most children have severe developmental delay and infantile spasms, but milder phenotypes are on record, including posterior SBH owing to mosaic mutations of LIS1.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP606032.RA0_cQkdYe-gRo1a8jrYcYtdMqfmHdJ7OBxOLbHbWw10s130_provenance.
- NP606032.RA0_cQkdYe-gRo1a8jrYcYtdMqfmHdJ7OBxOLbHbWw10s130_assertion evidence source_evidence_literature NP606032.RA0_cQkdYe-gRo1a8jrYcYtdMqfmHdJ7OBxOLbHbWw10s130_provenance.
- NP606032.RA0_cQkdYe-gRo1a8jrYcYtdMqfmHdJ7OBxOLbHbWw10s130_assertion SIO_000772 16724181 NP606032.RA0_cQkdYe-gRo1a8jrYcYtdMqfmHdJ7OBxOLbHbWw10s130_provenance.
- NP606032.RA0_cQkdYe-gRo1a8jrYcYtdMqfmHdJ7OBxOLbHbWw10s130_assertion wasDerivedFrom befree-20150227 NP606032.RA0_cQkdYe-gRo1a8jrYcYtdMqfmHdJ7OBxOLbHbWw10s130_provenance.
- NP606032.RA0_cQkdYe-gRo1a8jrYcYtdMqfmHdJ7OBxOLbHbWw10s130_assertion wasGeneratedBy ECO_0000203 NP606032.RA0_cQkdYe-gRo1a8jrYcYtdMqfmHdJ7OBxOLbHbWw10s130_provenance.