Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP452772.RAYwM-r-La_PL8EBHqU-DdHivKlrPGgJateL9eCWSyUbo130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP452772.RAYwM-r-La_PL8EBHqU-DdHivKlrPGgJateL9eCWSyUbo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP452772.RAYwM-r-La_PL8EBHqU-DdHivKlrPGgJateL9eCWSyUbo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP452772.RAYwM-r-La_PL8EBHqU-DdHivKlrPGgJateL9eCWSyUbo130_provenance.
- NP452772.RAYwM-r-La_PL8EBHqU-DdHivKlrPGgJateL9eCWSyUbo130_assertion wasGeneratedBy ECO_0000203 NP452772.RAYwM-r-La_PL8EBHqU-DdHivKlrPGgJateL9eCWSyUbo130_provenance.
- NP452772.RAYwM-r-La_PL8EBHqU-DdHivKlrPGgJateL9eCWSyUbo130_assertion wasDerivedFrom befree-20140225 NP452772.RAYwM-r-La_PL8EBHqU-DdHivKlrPGgJateL9eCWSyUbo130_provenance.
- NP452772.RAYwM-r-La_PL8EBHqU-DdHivKlrPGgJateL9eCWSyUbo130_assertion SIO_000772 11254445 NP452772.RAYwM-r-La_PL8EBHqU-DdHivKlrPGgJateL9eCWSyUbo130_provenance.
- NP452772.RAYwM-r-La_PL8EBHqU-DdHivKlrPGgJateL9eCWSyUbo130_assertion evidence source_evidence_literature NP452772.RAYwM-r-La_PL8EBHqU-DdHivKlrPGgJateL9eCWSyUbo130_provenance.
- NP452772.RAYwM-r-La_PL8EBHqU-DdHivKlrPGgJateL9eCWSyUbo130_assertion description "[To assess the contribution that SCN1A makes to other types of epilepsy, 226 patients with either juvenile myoclonic epilepsy, absence epilepsy, or febrile convulsions were screened by conformation-sensitive gel electrophoresis and manual sequencing of variants; the sample included 165 probands from multiplex families and 61 sporadic cases.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP452772.RAYwM-r-La_PL8EBHqU-DdHivKlrPGgJateL9eCWSyUbo130_provenance.
- befree-20140225 importedOn "2014-02-25" NP452772.RAYwM-r-La_PL8EBHqU-DdHivKlrPGgJateL9eCWSyUbo130_provenance.