Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP316670.RA9SaU2hTp81_ID1XNV98Nket3DtOePswouygxiAU-deM130_assertion> ?p ?o ?g. }
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- NP316670.RA9SaU2hTp81_ID1XNV98Nket3DtOePswouygxiAU-deM130_assertion type Assertion NP316670.RA9SaU2hTp81_ID1XNV98Nket3DtOePswouygxiAU-deM130_head.
- NP316670.RA9SaU2hTp81_ID1XNV98Nket3DtOePswouygxiAU-deM130_assertion description "[To identify suspected RDS mutations in families in which different people have been identified with either generalised retinal dystrophy or macular dystrophy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP316670.RA9SaU2hTp81_ID1XNV98Nket3DtOePswouygxiAU-deM130_provenance.
- NP316670.RA9SaU2hTp81_ID1XNV98Nket3DtOePswouygxiAU-deM130_assertion evidence source_evidence_literature NP316670.RA9SaU2hTp81_ID1XNV98Nket3DtOePswouygxiAU-deM130_provenance.
- NP316670.RA9SaU2hTp81_ID1XNV98Nket3DtOePswouygxiAU-deM130_assertion SIO_000772 16916875 NP316670.RA9SaU2hTp81_ID1XNV98Nket3DtOePswouygxiAU-deM130_provenance.
- NP316670.RA9SaU2hTp81_ID1XNV98Nket3DtOePswouygxiAU-deM130_assertion wasDerivedFrom befree-20140225 NP316670.RA9SaU2hTp81_ID1XNV98Nket3DtOePswouygxiAU-deM130_provenance.
- NP316670.RA9SaU2hTp81_ID1XNV98Nket3DtOePswouygxiAU-deM130_assertion wasGeneratedBy ECO_0000203 NP316670.RA9SaU2hTp81_ID1XNV98Nket3DtOePswouygxiAU-deM130_provenance.