Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP511534.RARI8rjjqHJNEQWtqccJA9qa5jDshSCvWq1OgW_XssfZg130_assertion> ?p ?o ?g. }
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- NP511534.RARI8rjjqHJNEQWtqccJA9qa5jDshSCvWq1OgW_XssfZg130_assertion type Assertion NP511534.RARI8rjjqHJNEQWtqccJA9qa5jDshSCvWq1OgW_XssfZg130_head.
- NP511534.RARI8rjjqHJNEQWtqccJA9qa5jDshSCvWq1OgW_XssfZg130_assertion description "[Three human diseases cosegregate with microsatellite markers used in construction of the human BAC/YAC physical map, including autosomal dominant nocturnal frontal lobe epilepsy (ENFL2; also known as ADNFLE), a syndrome of mental retardation, spasticity, and tapetoretinal degeneration (MRST); and a pyogenic arthritis, pyoderma gangrenosum, and acne syndrome (PAPA).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP511534.RARI8rjjqHJNEQWtqccJA9qa5jDshSCvWq1OgW_XssfZg130_provenance.
- NP511534.RARI8rjjqHJNEQWtqccJA9qa5jDshSCvWq1OgW_XssfZg130_assertion evidence source_evidence_literature NP511534.RARI8rjjqHJNEQWtqccJA9qa5jDshSCvWq1OgW_XssfZg130_provenance.
- NP511534.RARI8rjjqHJNEQWtqccJA9qa5jDshSCvWq1OgW_XssfZg130_assertion SIO_000772 11247670 NP511534.RARI8rjjqHJNEQWtqccJA9qa5jDshSCvWq1OgW_XssfZg130_provenance.
- NP511534.RARI8rjjqHJNEQWtqccJA9qa5jDshSCvWq1OgW_XssfZg130_assertion wasDerivedFrom befree-20140225 NP511534.RARI8rjjqHJNEQWtqccJA9qa5jDshSCvWq1OgW_XssfZg130_provenance.
- NP511534.RARI8rjjqHJNEQWtqccJA9qa5jDshSCvWq1OgW_XssfZg130_assertion wasGeneratedBy ECO_0000203 NP511534.RARI8rjjqHJNEQWtqccJA9qa5jDshSCvWq1OgW_XssfZg130_provenance.