Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1249183.RAn5U_EpKJ8Xl76eByZ88x_4xsx6HdWaWC3GZddeD2urw130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP1249183.RAn5U_EpKJ8Xl76eByZ88x_4xsx6HdWaWC3GZddeD2urw130_assertion type Assertion NP1249183.RAn5U_EpKJ8Xl76eByZ88x_4xsx6HdWaWC3GZddeD2urw130_head.
- NP1249183.RAn5U_EpKJ8Xl76eByZ88x_4xsx6HdWaWC3GZddeD2urw130_assertion description "[Mutations in KATNB1 cause complex cerebral malformations by disrupting asymmetrically dividing neural progenitors.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1249183.RAn5U_EpKJ8Xl76eByZ88x_4xsx6HdWaWC3GZddeD2urw130_provenance.
- NP1249183.RAn5U_EpKJ8Xl76eByZ88x_4xsx6HdWaWC3GZddeD2urw130_assertion evidence source_evidence_literature NP1249183.RAn5U_EpKJ8Xl76eByZ88x_4xsx6HdWaWC3GZddeD2urw130_provenance.
- NP1249183.RAn5U_EpKJ8Xl76eByZ88x_4xsx6HdWaWC3GZddeD2urw130_assertion SIO_000772 25521378 NP1249183.RAn5U_EpKJ8Xl76eByZ88x_4xsx6HdWaWC3GZddeD2urw130_provenance.
- NP1249183.RAn5U_EpKJ8Xl76eByZ88x_4xsx6HdWaWC3GZddeD2urw130_assertion wasDerivedFrom befree-2016 NP1249183.RAn5U_EpKJ8Xl76eByZ88x_4xsx6HdWaWC3GZddeD2urw130_provenance.
- NP1249183.RAn5U_EpKJ8Xl76eByZ88x_4xsx6HdWaWC3GZddeD2urw130_assertion wasGeneratedBy ECO_0000203 NP1249183.RAn5U_EpKJ8Xl76eByZ88x_4xsx6HdWaWC3GZddeD2urw130_provenance.