Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP606199.RAuWrSV2otfRWdXDAzZe2QgNAuHiydpPuOmb7cDykqBMk130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP606199.RAuWrSV2otfRWdXDAzZe2QgNAuHiydpPuOmb7cDykqBMk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP606199.RAuWrSV2otfRWdXDAzZe2QgNAuHiydpPuOmb7cDykqBMk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP606199.RAuWrSV2otfRWdXDAzZe2QgNAuHiydpPuOmb7cDykqBMk130_provenance.
- NP606199.RAuWrSV2otfRWdXDAzZe2QgNAuHiydpPuOmb7cDykqBMk130_assertion description "[Most children have severe developmental delay and infantile spasms, but milder phenotypes are on record, including posterior SBH owing to mosaic mutations of LIS1.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP606199.RAuWrSV2otfRWdXDAzZe2QgNAuHiydpPuOmb7cDykqBMk130_provenance.
- NP606199.RAuWrSV2otfRWdXDAzZe2QgNAuHiydpPuOmb7cDykqBMk130_assertion evidence source_evidence_literature NP606199.RAuWrSV2otfRWdXDAzZe2QgNAuHiydpPuOmb7cDykqBMk130_provenance.
- NP606199.RAuWrSV2otfRWdXDAzZe2QgNAuHiydpPuOmb7cDykqBMk130_assertion SIO_000772 16724181 NP606199.RAuWrSV2otfRWdXDAzZe2QgNAuHiydpPuOmb7cDykqBMk130_provenance.
- NP606199.RAuWrSV2otfRWdXDAzZe2QgNAuHiydpPuOmb7cDykqBMk130_assertion wasDerivedFrom befree-20150227 NP606199.RAuWrSV2otfRWdXDAzZe2QgNAuHiydpPuOmb7cDykqBMk130_provenance.
- NP606199.RAuWrSV2otfRWdXDAzZe2QgNAuHiydpPuOmb7cDykqBMk130_assertion wasGeneratedBy ECO_0000203 NP606199.RAuWrSV2otfRWdXDAzZe2QgNAuHiydpPuOmb7cDykqBMk130_provenance.
- befree-20150227 importedOn "2015-02-27" NP606199.RAuWrSV2otfRWdXDAzZe2QgNAuHiydpPuOmb7cDykqBMk130_provenance.