Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP838800.RAABHZT_HTZEKlmoBRfP1RSIEybEtigHpFyN-84c5Khl8130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP838800.RAABHZT_HTZEKlmoBRfP1RSIEybEtigHpFyN-84c5Khl8130_assertion type Assertion NP838800.RAABHZT_HTZEKlmoBRfP1RSIEybEtigHpFyN-84c5Khl8130_head.
- NP838800.RAABHZT_HTZEKlmoBRfP1RSIEybEtigHpFyN-84c5Khl8130_assertion description "[Meckel-Gruber syndrome type 3 (MKS3; OMIM 607361) is a severe autosomal recessive disorder characterized by bilateral polycystic kidney disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP838800.RAABHZT_HTZEKlmoBRfP1RSIEybEtigHpFyN-84c5Khl8130_provenance.
- NP838800.RAABHZT_HTZEKlmoBRfP1RSIEybEtigHpFyN-84c5Khl8130_assertion evidence source_evidence_literature NP838800.RAABHZT_HTZEKlmoBRfP1RSIEybEtigHpFyN-84c5Khl8130_provenance.
- NP838800.RAABHZT_HTZEKlmoBRfP1RSIEybEtigHpFyN-84c5Khl8130_assertion SIO_000772 19211713 NP838800.RAABHZT_HTZEKlmoBRfP1RSIEybEtigHpFyN-84c5Khl8130_provenance.
- NP838800.RAABHZT_HTZEKlmoBRfP1RSIEybEtigHpFyN-84c5Khl8130_assertion wasDerivedFrom befree-20140225 NP838800.RAABHZT_HTZEKlmoBRfP1RSIEybEtigHpFyN-84c5Khl8130_provenance.
- NP838800.RAABHZT_HTZEKlmoBRfP1RSIEybEtigHpFyN-84c5Khl8130_assertion wasGeneratedBy ECO_0000203 NP838800.RAABHZT_HTZEKlmoBRfP1RSIEybEtigHpFyN-84c5Khl8130_provenance.