Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP350670.RAS1zvDDE06axM_M4Y33rJv6F60yN4ysCo0iiyAOcWrv4130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP350670.RAS1zvDDE06axM_M4Y33rJv6F60yN4ysCo0iiyAOcWrv4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP350670.RAS1zvDDE06axM_M4Y33rJv6F60yN4ysCo0iiyAOcWrv4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP350670.RAS1zvDDE06axM_M4Y33rJv6F60yN4ysCo0iiyAOcWrv4130_provenance.
- NP350670.RAS1zvDDE06axM_M4Y33rJv6F60yN4ysCo0iiyAOcWrv4130_assertion description "[In human patients, cortical dysplasia produced by Doublecortin (DCX) mutations lead to mental retardation and intractable infantile epilepsies, but the underlying mechanisms are not known.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP350670.RAS1zvDDE06axM_M4Y33rJv6F60yN4ysCo0iiyAOcWrv4130_provenance.
- NP350670.RAS1zvDDE06axM_M4Y33rJv6F60yN4ysCo0iiyAOcWrv4130_assertion evidence source_evidence_literature NP350670.RAS1zvDDE06axM_M4Y33rJv6F60yN4ysCo0iiyAOcWrv4130_provenance.
- NP350670.RAS1zvDDE06axM_M4Y33rJv6F60yN4ysCo0iiyAOcWrv4130_assertion SIO_000772 19144832 NP350670.RAS1zvDDE06axM_M4Y33rJv6F60yN4ysCo0iiyAOcWrv4130_provenance.
- NP350670.RAS1zvDDE06axM_M4Y33rJv6F60yN4ysCo0iiyAOcWrv4130_assertion wasDerivedFrom befree-20150227 NP350670.RAS1zvDDE06axM_M4Y33rJv6F60yN4ysCo0iiyAOcWrv4130_provenance.
- NP350670.RAS1zvDDE06axM_M4Y33rJv6F60yN4ysCo0iiyAOcWrv4130_assertion wasGeneratedBy ECO_0000203 NP350670.RAS1zvDDE06axM_M4Y33rJv6F60yN4ysCo0iiyAOcWrv4130_provenance.
- befree-20150227 importedOn "2015-02-27" NP350670.RAS1zvDDE06axM_M4Y33rJv6F60yN4ysCo0iiyAOcWrv4130_provenance.