Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP606080.RA9toIKs4gblBu-DagV6BJW6KjLHCFG0KfPYWaFDZcMeM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP606080.RA9toIKs4gblBu-DagV6BJW6KjLHCFG0KfPYWaFDZcMeM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP606080.RA9toIKs4gblBu-DagV6BJW6KjLHCFG0KfPYWaFDZcMeM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP606080.RA9toIKs4gblBu-DagV6BJW6KjLHCFG0KfPYWaFDZcMeM130_provenance.
- NP606080.RA9toIKs4gblBu-DagV6BJW6KjLHCFG0KfPYWaFDZcMeM130_assertion description "[Mutation analysis of LIS1, using highly sensitive techniques such as denaturing high-pressure liquid chromatography, should be considered for patients with posteriorly predominant subcortical band heterotopia and pachygyria.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP606080.RA9toIKs4gblBu-DagV6BJW6KjLHCFG0KfPYWaFDZcMeM130_provenance.
- NP606080.RA9toIKs4gblBu-DagV6BJW6KjLHCFG0KfPYWaFDZcMeM130_assertion evidence source_evidence_literature NP606080.RA9toIKs4gblBu-DagV6BJW6KjLHCFG0KfPYWaFDZcMeM130_provenance.
- NP606080.RA9toIKs4gblBu-DagV6BJW6KjLHCFG0KfPYWaFDZcMeM130_assertion SIO_000772 14581661 NP606080.RA9toIKs4gblBu-DagV6BJW6KjLHCFG0KfPYWaFDZcMeM130_provenance.
- NP606080.RA9toIKs4gblBu-DagV6BJW6KjLHCFG0KfPYWaFDZcMeM130_assertion wasDerivedFrom befree-20150227 NP606080.RA9toIKs4gblBu-DagV6BJW6KjLHCFG0KfPYWaFDZcMeM130_provenance.
- NP606080.RA9toIKs4gblBu-DagV6BJW6KjLHCFG0KfPYWaFDZcMeM130_assertion wasGeneratedBy ECO_0000203 NP606080.RA9toIKs4gblBu-DagV6BJW6KjLHCFG0KfPYWaFDZcMeM130_provenance.
- befree-20150227 importedOn "2015-02-27" NP606080.RA9toIKs4gblBu-DagV6BJW6KjLHCFG0KfPYWaFDZcMeM130_provenance.