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- NP767551.RAIik_JWIH7ZyhIC0Y_vHIspbnv4HkXwhXVc8fc4Tf-jY130_assertion type Assertion NP767551.RAIik_JWIH7ZyhIC0Y_vHIspbnv4HkXwhXVc8fc4Tf-jY130_head.
- NP767551.RAIik_JWIH7ZyhIC0Y_vHIspbnv4HkXwhXVc8fc4Tf-jY130_assertion wasGeneratedBy ECO_0000203 NP767551.RAIik_JWIH7ZyhIC0Y_vHIspbnv4HkXwhXVc8fc4Tf-jY130_provenance.
- NP767551.RAIik_JWIH7ZyhIC0Y_vHIspbnv4HkXwhXVc8fc4Tf-jY130_assertion wasDerivedFrom befree-20150227 NP767551.RAIik_JWIH7ZyhIC0Y_vHIspbnv4HkXwhXVc8fc4Tf-jY130_provenance.
- NP767551.RAIik_JWIH7ZyhIC0Y_vHIspbnv4HkXwhXVc8fc4Tf-jY130_assertion SIO_000772 22004887 NP767551.RAIik_JWIH7ZyhIC0Y_vHIspbnv4HkXwhXVc8fc4Tf-jY130_provenance.
- NP767551.RAIik_JWIH7ZyhIC0Y_vHIspbnv4HkXwhXVc8fc4Tf-jY130_assertion evidence source_evidence_literature NP767551.RAIik_JWIH7ZyhIC0Y_vHIspbnv4HkXwhXVc8fc4Tf-jY130_provenance.
- NP767551.RAIik_JWIH7ZyhIC0Y_vHIspbnv4HkXwhXVc8fc4Tf-jY130_assertion description "[This report provide a wide spectrum of USH2A mutations and clinical features, including atypical Usher syndrome phenotypes resembling Usher syndrome type I.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP767551.RAIik_JWIH7ZyhIC0Y_vHIspbnv4HkXwhXVc8fc4Tf-jY130_provenance.