Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP367167.RA-GY-gLm1a_3fh6PwNDPjzRvmakUK8vjTcDdKl4uksVY130_assertion> ?p ?o ?g. }
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- NP367167.RA-GY-gLm1a_3fh6PwNDPjzRvmakUK8vjTcDdKl4uksVY130_assertion type Assertion NP367167.RA-GY-gLm1a_3fh6PwNDPjzRvmakUK8vjTcDdKl4uksVY130_head.
- NP367167.RA-GY-gLm1a_3fh6PwNDPjzRvmakUK8vjTcDdKl4uksVY130_assertion description "[Two families with a retinal dystrophy were extensively phenotyped and blood was taken for mutation analysis of the RDS (all) and ROM1 (retinitis pigmentosa patients only) genes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP367167.RA-GY-gLm1a_3fh6PwNDPjzRvmakUK8vjTcDdKl4uksVY130_provenance.
- NP367167.RA-GY-gLm1a_3fh6PwNDPjzRvmakUK8vjTcDdKl4uksVY130_assertion evidence source_evidence_literature NP367167.RA-GY-gLm1a_3fh6PwNDPjzRvmakUK8vjTcDdKl4uksVY130_provenance.
- NP367167.RA-GY-gLm1a_3fh6PwNDPjzRvmakUK8vjTcDdKl4uksVY130_assertion SIO_000772 16916875 NP367167.RA-GY-gLm1a_3fh6PwNDPjzRvmakUK8vjTcDdKl4uksVY130_provenance.
- NP367167.RA-GY-gLm1a_3fh6PwNDPjzRvmakUK8vjTcDdKl4uksVY130_assertion wasDerivedFrom befree-20140225 NP367167.RA-GY-gLm1a_3fh6PwNDPjzRvmakUK8vjTcDdKl4uksVY130_provenance.
- NP367167.RA-GY-gLm1a_3fh6PwNDPjzRvmakUK8vjTcDdKl4uksVY130_assertion wasGeneratedBy ECO_0000203 NP367167.RA-GY-gLm1a_3fh6PwNDPjzRvmakUK8vjTcDdKl4uksVY130_provenance.