Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP545311.RAU87U9Mfrt6FCU-_yaq4UfGs9x2LVC1axrhL4ez7529c130_assertion> ?p ?o ?g. }
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- NP545311.RAU87U9Mfrt6FCU-_yaq4UfGs9x2LVC1axrhL4ez7529c130_assertion type Assertion NP545311.RAU87U9Mfrt6FCU-_yaq4UfGs9x2LVC1axrhL4ez7529c130_head.
- NP545311.RAU87U9Mfrt6FCU-_yaq4UfGs9x2LVC1axrhL4ez7529c130_assertion description "[Analysis of a 43.6 kb deletion in a patient with Hunter syndrome (MPSII): identification of a fusion transcript including sequences from the gene W and the IDS gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP545311.RAU87U9Mfrt6FCU-_yaq4UfGs9x2LVC1axrhL4ez7529c130_provenance.
- NP545311.RAU87U9Mfrt6FCU-_yaq4UfGs9x2LVC1axrhL4ez7529c130_assertion evidence source_evidence_literature NP545311.RAU87U9Mfrt6FCU-_yaq4UfGs9x2LVC1axrhL4ez7529c130_provenance.
- NP545311.RAU87U9Mfrt6FCU-_yaq4UfGs9x2LVC1axrhL4ez7529c130_assertion SIO_000772 10737977 NP545311.RAU87U9Mfrt6FCU-_yaq4UfGs9x2LVC1axrhL4ez7529c130_provenance.
- NP545311.RAU87U9Mfrt6FCU-_yaq4UfGs9x2LVC1axrhL4ez7529c130_assertion wasDerivedFrom befree-20140225 NP545311.RAU87U9Mfrt6FCU-_yaq4UfGs9x2LVC1axrhL4ez7529c130_provenance.
- NP545311.RAU87U9Mfrt6FCU-_yaq4UfGs9x2LVC1axrhL4ez7529c130_assertion wasGeneratedBy ECO_0000203 NP545311.RAU87U9Mfrt6FCU-_yaq4UfGs9x2LVC1axrhL4ez7529c130_provenance.