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- NP536932.RA1J0fbtG9kadzQfzXhcRIPJc7D6mfqXEGqFO6g2UbII8130_assertion type Assertion NP536932.RA1J0fbtG9kadzQfzXhcRIPJc7D6mfqXEGqFO6g2UbII8130_head.
- NP536932.RA1J0fbtG9kadzQfzXhcRIPJc7D6mfqXEGqFO6g2UbII8130_assertion wasGeneratedBy ECO_0000203 NP536932.RA1J0fbtG9kadzQfzXhcRIPJc7D6mfqXEGqFO6g2UbII8130_provenance.
- NP536932.RA1J0fbtG9kadzQfzXhcRIPJc7D6mfqXEGqFO6g2UbII8130_assertion wasDerivedFrom befree-20140225 NP536932.RA1J0fbtG9kadzQfzXhcRIPJc7D6mfqXEGqFO6g2UbII8130_provenance.
- NP536932.RA1J0fbtG9kadzQfzXhcRIPJc7D6mfqXEGqFO6g2UbII8130_assertion SIO_000772 20234391 NP536932.RA1J0fbtG9kadzQfzXhcRIPJc7D6mfqXEGqFO6g2UbII8130_provenance.
- NP536932.RA1J0fbtG9kadzQfzXhcRIPJc7D6mfqXEGqFO6g2UbII8130_assertion evidence source_evidence_literature NP536932.RA1J0fbtG9kadzQfzXhcRIPJc7D6mfqXEGqFO6g2UbII8130_provenance.
- NP536932.RA1J0fbtG9kadzQfzXhcRIPJc7D6mfqXEGqFO6g2UbII8130_assertion description "[Heterozygous deletion of a 2-Mb region including the dystroglycan gene in a patient with mild myopathy, facial hypotonia, oral-motor dyspraxia and white matter abnormalities.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP536932.RA1J0fbtG9kadzQfzXhcRIPJc7D6mfqXEGqFO6g2UbII8130_provenance.