Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP24288.RA8k1_cGiHTSn6d17EGODENOh3ALB6QZf-ZFjNT2HLcR4130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP24288.RA8k1_cGiHTSn6d17EGODENOh3ALB6QZf-ZFjNT2HLcR4130_assertion type Assertion NP24288.RA8k1_cGiHTSn6d17EGODENOh3ALB6QZf-ZFjNT2HLcR4130_head.
- NP24288.RA8k1_cGiHTSn6d17EGODENOh3ALB6QZf-ZFjNT2HLcR4130_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." NP24288.RA8k1_cGiHTSn6d17EGODENOh3ALB6QZf-ZFjNT2HLcR4130_provenance.
- NP24288.RA8k1_cGiHTSn6d17EGODENOh3ALB6QZf-ZFjNT2HLcR4130_assertion evidence source_evidence_curated NP24288.RA8k1_cGiHTSn6d17EGODENOh3ALB6QZf-ZFjNT2HLcR4130_provenance.
- NP24288.RA8k1_cGiHTSn6d17EGODENOh3ALB6QZf-ZFjNT2HLcR4130_assertion SIO_000772 19559301 NP24288.RA8k1_cGiHTSn6d17EGODENOh3ALB6QZf-ZFjNT2HLcR4130_provenance.
- NP24288.RA8k1_cGiHTSn6d17EGODENOh3ALB6QZf-ZFjNT2HLcR4130_assertion wasDerivedFrom ctd_human-2016 NP24288.RA8k1_cGiHTSn6d17EGODENOh3ALB6QZf-ZFjNT2HLcR4130_provenance.
- NP24288.RA8k1_cGiHTSn6d17EGODENOh3ALB6QZf-ZFjNT2HLcR4130_assertion wasGeneratedBy ECO_0000218 NP24288.RA8k1_cGiHTSn6d17EGODENOh3ALB6QZf-ZFjNT2HLcR4130_provenance.