Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP5004.RARUN1zsO2OhrTEgcjxsEWzJ1sQnR0EqcIQEwfM6uuC2g130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP5004.RARUN1zsO2OhrTEgcjxsEWzJ1sQnR0EqcIQEwfM6uuC2g130_assertion type Assertion NP5004.RARUN1zsO2OhrTEgcjxsEWzJ1sQnR0EqcIQEwfM6uuC2g130_head.
- NP5004.RARUN1zsO2OhrTEgcjxsEWzJ1sQnR0EqcIQEwfM6uuC2g130_assertion description "[Hypomorphic mutations in PGAP2, encoding a GPI-anchor-remodeling protein, cause autosomal-recessive intellectual disability.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP5004.RARUN1zsO2OhrTEgcjxsEWzJ1sQnR0EqcIQEwfM6uuC2g130_provenance.
- NP5004.RARUN1zsO2OhrTEgcjxsEWzJ1sQnR0EqcIQEwfM6uuC2g130_assertion evidence source_evidence_curated NP5004.RARUN1zsO2OhrTEgcjxsEWzJ1sQnR0EqcIQEwfM6uuC2g130_provenance.
- NP5004.RARUN1zsO2OhrTEgcjxsEWzJ1sQnR0EqcIQEwfM6uuC2g130_assertion SIO_000772 23561846 NP5004.RARUN1zsO2OhrTEgcjxsEWzJ1sQnR0EqcIQEwfM6uuC2g130_provenance.
- NP5004.RARUN1zsO2OhrTEgcjxsEWzJ1sQnR0EqcIQEwfM6uuC2g130_assertion wasDerivedFrom uniprot-20150221 NP5004.RARUN1zsO2OhrTEgcjxsEWzJ1sQnR0EqcIQEwfM6uuC2g130_provenance.
- NP5004.RARUN1zsO2OhrTEgcjxsEWzJ1sQnR0EqcIQEwfM6uuC2g130_assertion wasGeneratedBy ECO_0000218 NP5004.RARUN1zsO2OhrTEgcjxsEWzJ1sQnR0EqcIQEwfM6uuC2g130_provenance.