Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP24286.RA8S3v1AiFg-m2ri1ZBA37gzETDou3-gzOrsBeq5n8g_s130_assertion> ?p ?o ?g. }
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- NP24286.RA8S3v1AiFg-m2ri1ZBA37gzETDou3-gzOrsBeq5n8g_s130_assertion type Assertion NP24286.RA8S3v1AiFg-m2ri1ZBA37gzETDou3-gzOrsBeq5n8g_s130_head.
- NP24286.RA8S3v1AiFg-m2ri1ZBA37gzETDou3-gzOrsBeq5n8g_s130_assertion description "[A novel MECP2 mutation in a boy with neonatal encephalopathy and facial dysmorphism.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP24286.RA8S3v1AiFg-m2ri1ZBA37gzETDou3-gzOrsBeq5n8g_s130_provenance.
- NP24286.RA8S3v1AiFg-m2ri1ZBA37gzETDou3-gzOrsBeq5n8g_s130_assertion evidence source_evidence_curated NP24286.RA8S3v1AiFg-m2ri1ZBA37gzETDou3-gzOrsBeq5n8g_s130_provenance.
- NP24286.RA8S3v1AiFg-m2ri1ZBA37gzETDou3-gzOrsBeq5n8g_s130_assertion SIO_000772 19559301 NP24286.RA8S3v1AiFg-m2ri1ZBA37gzETDou3-gzOrsBeq5n8g_s130_provenance.
- NP24286.RA8S3v1AiFg-m2ri1ZBA37gzETDou3-gzOrsBeq5n8g_s130_assertion wasDerivedFrom ctd_human-2016 NP24286.RA8S3v1AiFg-m2ri1ZBA37gzETDou3-gzOrsBeq5n8g_s130_provenance.
- NP24286.RA8S3v1AiFg-m2ri1ZBA37gzETDou3-gzOrsBeq5n8g_s130_assertion wasGeneratedBy ECO_0000218 NP24286.RA8S3v1AiFg-m2ri1ZBA37gzETDou3-gzOrsBeq5n8g_s130_provenance.