Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP721134.RAJhBz6eM4O5CA7STNxeIb1NmgKsu_EHdLghLJHss33a0130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP721134.RAJhBz6eM4O5CA7STNxeIb1NmgKsu_EHdLghLJHss33a0130_assertion type Assertion NP721134.RAJhBz6eM4O5CA7STNxeIb1NmgKsu_EHdLghLJHss33a0130_head.
- NP721134.RAJhBz6eM4O5CA7STNxeIb1NmgKsu_EHdLghLJHss33a0130_assertion description "[Autosomal recessive Meckel syndrome (OMIM 249000) (MES), first described in 1822 by Johann F. Meckel, is a major monogenic malformation syndrome with a neural tube defect leading to death of the fetus in utero or shortly after birth.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP721134.RAJhBz6eM4O5CA7STNxeIb1NmgKsu_EHdLghLJHss33a0130_provenance.
- NP721134.RAJhBz6eM4O5CA7STNxeIb1NmgKsu_EHdLghLJHss33a0130_assertion evidence source_evidence_literature NP721134.RAJhBz6eM4O5CA7STNxeIb1NmgKsu_EHdLghLJHss33a0130_provenance.
- NP721134.RAJhBz6eM4O5CA7STNxeIb1NmgKsu_EHdLghLJHss33a0130_assertion SIO_000772 7550354 NP721134.RAJhBz6eM4O5CA7STNxeIb1NmgKsu_EHdLghLJHss33a0130_provenance.
- NP721134.RAJhBz6eM4O5CA7STNxeIb1NmgKsu_EHdLghLJHss33a0130_assertion wasDerivedFrom befree-20140225 NP721134.RAJhBz6eM4O5CA7STNxeIb1NmgKsu_EHdLghLJHss33a0130_provenance.
- NP721134.RAJhBz6eM4O5CA7STNxeIb1NmgKsu_EHdLghLJHss33a0130_assertion wasGeneratedBy ECO_0000203 NP721134.RAJhBz6eM4O5CA7STNxeIb1NmgKsu_EHdLghLJHss33a0130_provenance.