Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP804917.RADG86uofEZIQcaUzg7Dio9Kvqg4NTdnmjhEv-9-Ef-pw130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP804917.RADG86uofEZIQcaUzg7Dio9Kvqg4NTdnmjhEv-9-Ef-pw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP804917.RADG86uofEZIQcaUzg7Dio9Kvqg4NTdnmjhEv-9-Ef-pw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP804917.RADG86uofEZIQcaUzg7Dio9Kvqg4NTdnmjhEv-9-Ef-pw130_provenance.
- NP804917.RADG86uofEZIQcaUzg7Dio9Kvqg4NTdnmjhEv-9-Ef-pw130_assertion description "[More recently, de novo missense mutations in the alpha-tubulin 1a gene (TUBA1A) located on chromosome 12q13.12, have also been associated with more or less severe defects of cortical development, resulting in complete agyria in the most severe cases of lissencephaly.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP804917.RADG86uofEZIQcaUzg7Dio9Kvqg4NTdnmjhEv-9-Ef-pw130_provenance.
- NP804917.RADG86uofEZIQcaUzg7Dio9Kvqg4NTdnmjhEv-9-Ef-pw130_assertion evidence source_evidence_literature NP804917.RADG86uofEZIQcaUzg7Dio9Kvqg4NTdnmjhEv-9-Ef-pw130_provenance.
- NP804917.RADG86uofEZIQcaUzg7Dio9Kvqg4NTdnmjhEv-9-Ef-pw130_assertion SIO_000772 20376468 NP804917.RADG86uofEZIQcaUzg7Dio9Kvqg4NTdnmjhEv-9-Ef-pw130_provenance.
- NP804917.RADG86uofEZIQcaUzg7Dio9Kvqg4NTdnmjhEv-9-Ef-pw130_assertion wasDerivedFrom befree-2016 NP804917.RADG86uofEZIQcaUzg7Dio9Kvqg4NTdnmjhEv-9-Ef-pw130_provenance.
- NP804917.RADG86uofEZIQcaUzg7Dio9Kvqg4NTdnmjhEv-9-Ef-pw130_assertion wasGeneratedBy ECO_0000203 NP804917.RADG86uofEZIQcaUzg7Dio9Kvqg4NTdnmjhEv-9-Ef-pw130_provenance.
- befree-2016 importedOn "2016-02-19" NP804917.RADG86uofEZIQcaUzg7Dio9Kvqg4NTdnmjhEv-9-Ef-pw130_provenance.