Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP247106.RAXUlGgbSY997_8bW9it-Lt5thQ-VPZebGv1XvIZ6_S2k130_assertion> ?p ?o ?g. }
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- NP247106.RAXUlGgbSY997_8bW9it-Lt5thQ-VPZebGv1XvIZ6_S2k130_assertion type Assertion NP247106.RAXUlGgbSY997_8bW9it-Lt5thQ-VPZebGv1XvIZ6_S2k130_head.
- NP247106.RAXUlGgbSY997_8bW9it-Lt5thQ-VPZebGv1XvIZ6_S2k130_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." NP247106.RAXUlGgbSY997_8bW9it-Lt5thQ-VPZebGv1XvIZ6_S2k130_provenance.
- NP247106.RAXUlGgbSY997_8bW9it-Lt5thQ-VPZebGv1XvIZ6_S2k130_assertion evidence source_evidence_literature NP247106.RAXUlGgbSY997_8bW9it-Lt5thQ-VPZebGv1XvIZ6_S2k130_provenance.
- NP247106.RAXUlGgbSY997_8bW9it-Lt5thQ-VPZebGv1XvIZ6_S2k130_assertion SIO_000772 16799052 NP247106.RAXUlGgbSY997_8bW9it-Lt5thQ-VPZebGv1XvIZ6_S2k130_provenance.
- NP247106.RAXUlGgbSY997_8bW9it-Lt5thQ-VPZebGv1XvIZ6_S2k130_assertion wasDerivedFrom befree-20140225 NP247106.RAXUlGgbSY997_8bW9it-Lt5thQ-VPZebGv1XvIZ6_S2k130_provenance.
- NP247106.RAXUlGgbSY997_8bW9it-Lt5thQ-VPZebGv1XvIZ6_S2k130_assertion wasGeneratedBy ECO_0000203 NP247106.RAXUlGgbSY997_8bW9it-Lt5thQ-VPZebGv1XvIZ6_S2k130_provenance.