Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP809204.RAem1vKJhf66QdeFpbNAE43xu3zEwUXpL-o-KSUqUjGvs130_assertion> ?p ?o ?g. }
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- NP809204.RAem1vKJhf66QdeFpbNAE43xu3zEwUXpL-o-KSUqUjGvs130_assertion type Assertion NP809204.RAem1vKJhf66QdeFpbNAE43xu3zEwUXpL-o-KSUqUjGvs130_head.
- NP809204.RAem1vKJhf66QdeFpbNAE43xu3zEwUXpL-o-KSUqUjGvs130_assertion description "[To examine the role of RP1 mutations in RP, we screened 101 unrelated Chinese RP patients (unselected for mode of inheritance) and 190 elderly normal control subjects for sequence changes in the coding exons for the 2156 amino acid RP1 protein.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP809204.RAem1vKJhf66QdeFpbNAE43xu3zEwUXpL-o-KSUqUjGvs130_provenance.
- NP809204.RAem1vKJhf66QdeFpbNAE43xu3zEwUXpL-o-KSUqUjGvs130_assertion evidence source_evidence_literature NP809204.RAem1vKJhf66QdeFpbNAE43xu3zEwUXpL-o-KSUqUjGvs130_provenance.
- NP809204.RAem1vKJhf66QdeFpbNAE43xu3zEwUXpL-o-KSUqUjGvs130_assertion SIO_000772 11317367 NP809204.RAem1vKJhf66QdeFpbNAE43xu3zEwUXpL-o-KSUqUjGvs130_provenance.
- NP809204.RAem1vKJhf66QdeFpbNAE43xu3zEwUXpL-o-KSUqUjGvs130_assertion wasDerivedFrom befree-20150227 NP809204.RAem1vKJhf66QdeFpbNAE43xu3zEwUXpL-o-KSUqUjGvs130_provenance.
- NP809204.RAem1vKJhf66QdeFpbNAE43xu3zEwUXpL-o-KSUqUjGvs130_assertion wasGeneratedBy ECO_0000203 NP809204.RAem1vKJhf66QdeFpbNAE43xu3zEwUXpL-o-KSUqUjGvs130_provenance.