Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP20289.RAvoD-jsaBe2nISAhroKT43l6EGGqPLiyoJPWUAEDVnMY130_assertion> ?p ?o ?g. }
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- NP20289.RAvoD-jsaBe2nISAhroKT43l6EGGqPLiyoJPWUAEDVnMY130_assertion type Assertion NP20289.RAvoD-jsaBe2nISAhroKT43l6EGGqPLiyoJPWUAEDVnMY130_head.
- NP20289.RAvoD-jsaBe2nISAhroKT43l6EGGqPLiyoJPWUAEDVnMY130_assertion description "[Deep sequencing reveals 50 novel genes for recessive cognitive disorders.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP20289.RAvoD-jsaBe2nISAhroKT43l6EGGqPLiyoJPWUAEDVnMY130_provenance.
- NP20289.RAvoD-jsaBe2nISAhroKT43l6EGGqPLiyoJPWUAEDVnMY130_assertion evidence source_evidence_curated NP20289.RAvoD-jsaBe2nISAhroKT43l6EGGqPLiyoJPWUAEDVnMY130_provenance.
- NP20289.RAvoD-jsaBe2nISAhroKT43l6EGGqPLiyoJPWUAEDVnMY130_assertion SIO_000772 21937992 NP20289.RAvoD-jsaBe2nISAhroKT43l6EGGqPLiyoJPWUAEDVnMY130_provenance.
- NP20289.RAvoD-jsaBe2nISAhroKT43l6EGGqPLiyoJPWUAEDVnMY130_assertion wasDerivedFrom ctd_human-20150221 NP20289.RAvoD-jsaBe2nISAhroKT43l6EGGqPLiyoJPWUAEDVnMY130_provenance.
- NP20289.RAvoD-jsaBe2nISAhroKT43l6EGGqPLiyoJPWUAEDVnMY130_assertion wasGeneratedBy ECO_0000218 NP20289.RAvoD-jsaBe2nISAhroKT43l6EGGqPLiyoJPWUAEDVnMY130_provenance.