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- source_evidence_literature type ECO_0000212 NP284929.RAyjuLjXxRS7Pun2zzpsQSkSPcP8gku7SMkFlPOpX_znA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP284929.RAyjuLjXxRS7Pun2zzpsQSkSPcP8gku7SMkFlPOpX_znA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP284929.RAyjuLjXxRS7Pun2zzpsQSkSPcP8gku7SMkFlPOpX_znA130_provenance.
- NP284929.RAyjuLjXxRS7Pun2zzpsQSkSPcP8gku7SMkFlPOpX_znA130_assertion description "[Mutations in the genes that encode filamin-1, Lis1 and doublecortin are responsible for X-linked lissencephaly in man, whereas mutations in the genes that encode Cdk5, its activator p35 and the reelin-signaling pathway disturb migration and architectonic development in mice.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP284929.RAyjuLjXxRS7Pun2zzpsQSkSPcP8gku7SMkFlPOpX_znA130_provenance.
- NP284929.RAyjuLjXxRS7Pun2zzpsQSkSPcP8gku7SMkFlPOpX_znA130_assertion evidence source_evidence_literature NP284929.RAyjuLjXxRS7Pun2zzpsQSkSPcP8gku7SMkFlPOpX_znA130_provenance.
- NP284929.RAyjuLjXxRS7Pun2zzpsQSkSPcP8gku7SMkFlPOpX_znA130_assertion SIO_000772 10826984 NP284929.RAyjuLjXxRS7Pun2zzpsQSkSPcP8gku7SMkFlPOpX_znA130_provenance.
- NP284929.RAyjuLjXxRS7Pun2zzpsQSkSPcP8gku7SMkFlPOpX_znA130_assertion wasDerivedFrom befree-2016 NP284929.RAyjuLjXxRS7Pun2zzpsQSkSPcP8gku7SMkFlPOpX_znA130_provenance.
- NP284929.RAyjuLjXxRS7Pun2zzpsQSkSPcP8gku7SMkFlPOpX_znA130_assertion wasGeneratedBy ECO_0000203 NP284929.RAyjuLjXxRS7Pun2zzpsQSkSPcP8gku7SMkFlPOpX_znA130_provenance.
- befree-2016 importedOn "2016-02-19" NP284929.RAyjuLjXxRS7Pun2zzpsQSkSPcP8gku7SMkFlPOpX_znA130_provenance.