Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP230725.RA7JOYug12XiqP47raQuvwTPZRCU6CcMv0Hnpuf6lCSyU130_assertion> ?p ?o ?g. }
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- NP230725.RA7JOYug12XiqP47raQuvwTPZRCU6CcMv0Hnpuf6lCSyU130_assertion type Assertion NP230725.RA7JOYug12XiqP47raQuvwTPZRCU6CcMv0Hnpuf6lCSyU130_head.
- NP230725.RA7JOYug12XiqP47raQuvwTPZRCU6CcMv0Hnpuf6lCSyU130_assertion description "[mutations in GPD1-L as a pathogenic cause for a small subset of sudden infant death syndrome via a secondary loss-of-function mechanism ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP230725.RA7JOYug12XiqP47raQuvwTPZRCU6CcMv0Hnpuf6lCSyU130_provenance.
- NP230725.RA7JOYug12XiqP47raQuvwTPZRCU6CcMv0Hnpuf6lCSyU130_assertion evidence source_evidence_literature NP230725.RA7JOYug12XiqP47raQuvwTPZRCU6CcMv0Hnpuf6lCSyU130_provenance.
- NP230725.RA7JOYug12XiqP47raQuvwTPZRCU6CcMv0Hnpuf6lCSyU130_assertion SIO_000772 17967976 NP230725.RA7JOYug12XiqP47raQuvwTPZRCU6CcMv0Hnpuf6lCSyU130_provenance.
- NP230725.RA7JOYug12XiqP47raQuvwTPZRCU6CcMv0Hnpuf6lCSyU130_assertion wasDerivedFrom lhgdn-20090331 NP230725.RA7JOYug12XiqP47raQuvwTPZRCU6CcMv0Hnpuf6lCSyU130_provenance.
- NP230725.RA7JOYug12XiqP47raQuvwTPZRCU6CcMv0Hnpuf6lCSyU130_assertion wasGeneratedBy ECO_0000203 NP230725.RA7JOYug12XiqP47raQuvwTPZRCU6CcMv0Hnpuf6lCSyU130_provenance.