Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP693408.RA_uE2iqEUhjJRcVHTbGHZk7MeuRE1YFzoaXpd4O6poAM130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP693408.RA_uE2iqEUhjJRcVHTbGHZk7MeuRE1YFzoaXpd4O6poAM130_assertion type Assertion NP693408.RA_uE2iqEUhjJRcVHTbGHZk7MeuRE1YFzoaXpd4O6poAM130_head.
- NP693408.RA_uE2iqEUhjJRcVHTbGHZk7MeuRE1YFzoaXpd4O6poAM130_assertion description "[Holoprosencephaly, sacral anomalies, and situs ambiguus in an infant with partial monosomy 7q/trisomy 2p and SHH and HLXB9 haploinsufficiency..]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP693408.RA_uE2iqEUhjJRcVHTbGHZk7MeuRE1YFzoaXpd4O6poAM130_provenance.
- NP693408.RA_uE2iqEUhjJRcVHTbGHZk7MeuRE1YFzoaXpd4O6poAM130_assertion evidence source_evidence_literature NP693408.RA_uE2iqEUhjJRcVHTbGHZk7MeuRE1YFzoaXpd4O6poAM130_provenance.
- NP693408.RA_uE2iqEUhjJRcVHTbGHZk7MeuRE1YFzoaXpd4O6poAM130_assertion SIO_000772 10852374 NP693408.RA_uE2iqEUhjJRcVHTbGHZk7MeuRE1YFzoaXpd4O6poAM130_provenance.
- NP693408.RA_uE2iqEUhjJRcVHTbGHZk7MeuRE1YFzoaXpd4O6poAM130_assertion wasDerivedFrom befree-20150227 NP693408.RA_uE2iqEUhjJRcVHTbGHZk7MeuRE1YFzoaXpd4O6poAM130_provenance.
- NP693408.RA_uE2iqEUhjJRcVHTbGHZk7MeuRE1YFzoaXpd4O6poAM130_assertion wasGeneratedBy ECO_0000203 NP693408.RA_uE2iqEUhjJRcVHTbGHZk7MeuRE1YFzoaXpd4O6poAM130_provenance.