Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP767529.RAklAD6KyQa5V7IaHs9_AEcETTrgcju5tuSkE3VAWST6Q130_assertion> ?p ?o ?g. }
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- NP767529.RAklAD6KyQa5V7IaHs9_AEcETTrgcju5tuSkE3VAWST6Q130_assertion type Assertion NP767529.RAklAD6KyQa5V7IaHs9_AEcETTrgcju5tuSkE3VAWST6Q130_head.
- NP767529.RAklAD6KyQa5V7IaHs9_AEcETTrgcju5tuSkE3VAWST6Q130_assertion description "[Mutations in the Usher syndrome type I causing genes are also recorded in non-syndromic hearing loss cases and mutations in USH2A in non-syndromic retinitis pigmentosa.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP767529.RAklAD6KyQa5V7IaHs9_AEcETTrgcju5tuSkE3VAWST6Q130_provenance.
- NP767529.RAklAD6KyQa5V7IaHs9_AEcETTrgcju5tuSkE3VAWST6Q130_assertion evidence source_evidence_literature NP767529.RAklAD6KyQa5V7IaHs9_AEcETTrgcju5tuSkE3VAWST6Q130_provenance.
- NP767529.RAklAD6KyQa5V7IaHs9_AEcETTrgcju5tuSkE3VAWST6Q130_assertion SIO_000772 18484607 NP767529.RAklAD6KyQa5V7IaHs9_AEcETTrgcju5tuSkE3VAWST6Q130_provenance.
- NP767529.RAklAD6KyQa5V7IaHs9_AEcETTrgcju5tuSkE3VAWST6Q130_assertion wasDerivedFrom befree-20150227 NP767529.RAklAD6KyQa5V7IaHs9_AEcETTrgcju5tuSkE3VAWST6Q130_provenance.
- NP767529.RAklAD6KyQa5V7IaHs9_AEcETTrgcju5tuSkE3VAWST6Q130_assertion wasGeneratedBy ECO_0000203 NP767529.RAklAD6KyQa5V7IaHs9_AEcETTrgcju5tuSkE3VAWST6Q130_provenance.