Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP449061.RAzLChaggprJ6Ikul9BTEfsYaLXGc5NwyMXkdAklYRnQw130_assertion> ?p ?o ?g. }
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- NP449061.RAzLChaggprJ6Ikul9BTEfsYaLXGc5NwyMXkdAklYRnQw130_assertion type Assertion NP449061.RAzLChaggprJ6Ikul9BTEfsYaLXGc5NwyMXkdAklYRnQw130_head.
- NP449061.RAzLChaggprJ6Ikul9BTEfsYaLXGc5NwyMXkdAklYRnQw130_assertion description "[Probands from each family were screened for mutations in 13 genes known to cause adRP: CA4, CRX, FSCN2, IMPDH1, NRL, PRPF3 (RP18), PRPF8 (RP13), PRPF31 (RP11), RDS, RHO, ROM1, RP1, and RP9.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP449061.RAzLChaggprJ6Ikul9BTEfsYaLXGc5NwyMXkdAklYRnQw130_provenance.
- NP449061.RAzLChaggprJ6Ikul9BTEfsYaLXGc5NwyMXkdAklYRnQw130_assertion evidence source_evidence_literature NP449061.RAzLChaggprJ6Ikul9BTEfsYaLXGc5NwyMXkdAklYRnQw130_provenance.
- NP449061.RAzLChaggprJ6Ikul9BTEfsYaLXGc5NwyMXkdAklYRnQw130_assertion SIO_000772 16799052 NP449061.RAzLChaggprJ6Ikul9BTEfsYaLXGc5NwyMXkdAklYRnQw130_provenance.
- NP449061.RAzLChaggprJ6Ikul9BTEfsYaLXGc5NwyMXkdAklYRnQw130_assertion wasDerivedFrom befree-20140225 NP449061.RAzLChaggprJ6Ikul9BTEfsYaLXGc5NwyMXkdAklYRnQw130_provenance.
- NP449061.RAzLChaggprJ6Ikul9BTEfsYaLXGc5NwyMXkdAklYRnQw130_assertion wasGeneratedBy ECO_0000203 NP449061.RAzLChaggprJ6Ikul9BTEfsYaLXGc5NwyMXkdAklYRnQw130_provenance.