Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP537782.RAKzkrvjSGgXqFmKjuSo8lhe8cbgcQkY2GMDVvsDl4izY130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP537782.RAKzkrvjSGgXqFmKjuSo8lhe8cbgcQkY2GMDVvsDl4izY130_assertion type Assertion NP537782.RAKzkrvjSGgXqFmKjuSo8lhe8cbgcQkY2GMDVvsDl4izY130_head.
- NP537782.RAKzkrvjSGgXqFmKjuSo8lhe8cbgcQkY2GMDVvsDl4izY130_assertion description "[Congenital muscular dystrophy with dropped head phenotype and cognitive impairment due to a novel mutation in the LMNA gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP537782.RAKzkrvjSGgXqFmKjuSo8lhe8cbgcQkY2GMDVvsDl4izY130_provenance.
- NP537782.RAKzkrvjSGgXqFmKjuSo8lhe8cbgcQkY2GMDVvsDl4izY130_assertion evidence source_evidence_literature NP537782.RAKzkrvjSGgXqFmKjuSo8lhe8cbgcQkY2GMDVvsDl4izY130_provenance.
- NP537782.RAKzkrvjSGgXqFmKjuSo8lhe8cbgcQkY2GMDVvsDl4izY130_assertion SIO_000772 24684859 NP537782.RAKzkrvjSGgXqFmKjuSo8lhe8cbgcQkY2GMDVvsDl4izY130_provenance.
- NP537782.RAKzkrvjSGgXqFmKjuSo8lhe8cbgcQkY2GMDVvsDl4izY130_assertion wasDerivedFrom befree-20150227 NP537782.RAKzkrvjSGgXqFmKjuSo8lhe8cbgcQkY2GMDVvsDl4izY130_provenance.
- NP537782.RAKzkrvjSGgXqFmKjuSo8lhe8cbgcQkY2GMDVvsDl4izY130_assertion wasGeneratedBy ECO_0000203 NP537782.RAKzkrvjSGgXqFmKjuSo8lhe8cbgcQkY2GMDVvsDl4izY130_provenance.