Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP750982.RAA3WvVADnyzaCW-N-SXz2FU7w6QL5Etqfv57eMW-yeaM130_assertion> ?p ?o ?g. }
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- NP750982.RAA3WvVADnyzaCW-N-SXz2FU7w6QL5Etqfv57eMW-yeaM130_assertion type Assertion NP750982.RAA3WvVADnyzaCW-N-SXz2FU7w6QL5Etqfv57eMW-yeaM130_head.
- NP750982.RAA3WvVADnyzaCW-N-SXz2FU7w6QL5Etqfv57eMW-yeaM130_assertion wasGeneratedBy ECO_0000203 NP750982.RAA3WvVADnyzaCW-N-SXz2FU7w6QL5Etqfv57eMW-yeaM130_provenance.
- NP750982.RAA3WvVADnyzaCW-N-SXz2FU7w6QL5Etqfv57eMW-yeaM130_assertion wasDerivedFrom befree-20140225 NP750982.RAA3WvVADnyzaCW-N-SXz2FU7w6QL5Etqfv57eMW-yeaM130_provenance.
- NP750982.RAA3WvVADnyzaCW-N-SXz2FU7w6QL5Etqfv57eMW-yeaM130_assertion SIO_000772 23018678 NP750982.RAA3WvVADnyzaCW-N-SXz2FU7w6QL5Etqfv57eMW-yeaM130_provenance.
- NP750982.RAA3WvVADnyzaCW-N-SXz2FU7w6QL5Etqfv57eMW-yeaM130_assertion evidence source_evidence_literature NP750982.RAA3WvVADnyzaCW-N-SXz2FU7w6QL5Etqfv57eMW-yeaM130_provenance.
- NP750982.RAA3WvVADnyzaCW-N-SXz2FU7w6QL5Etqfv57eMW-yeaM130_assertion description "[Mutations in CUL7, OBSL1 and CCDC8 in 3-M syndrome lead to disordered growth factor signalling.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP750982.RAA3WvVADnyzaCW-N-SXz2FU7w6QL5Etqfv57eMW-yeaM130_provenance.