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- NP478002.RAm_PV2Zk2VDYJPoq29HkVUqpYL06DDNdCcal1hyl1DMk130_assertion type Assertion NP478002.RAm_PV2Zk2VDYJPoq29HkVUqpYL06DDNdCcal1hyl1DMk130_head.
- NP478002.RAm_PV2Zk2VDYJPoq29HkVUqpYL06DDNdCcal1hyl1DMk130_assertion description "[To investigate the retinal disease expression in USH2C, the subtype of Usher syndrome type 2 recently shown to be caused by mutation in the VLGR1 gene, and compare results with those from USH2A, a more common cause of Usher syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP478002.RAm_PV2Zk2VDYJPoq29HkVUqpYL06DDNdCcal1hyl1DMk130_provenance.
- NP478002.RAm_PV2Zk2VDYJPoq29HkVUqpYL06DDNdCcal1hyl1DMk130_assertion evidence source_evidence_literature NP478002.RAm_PV2Zk2VDYJPoq29HkVUqpYL06DDNdCcal1hyl1DMk130_provenance.
- NP478002.RAm_PV2Zk2VDYJPoq29HkVUqpYL06DDNdCcal1hyl1DMk130_assertion SIO_000772 15671307 NP478002.RAm_PV2Zk2VDYJPoq29HkVUqpYL06DDNdCcal1hyl1DMk130_provenance.
- NP478002.RAm_PV2Zk2VDYJPoq29HkVUqpYL06DDNdCcal1hyl1DMk130_assertion wasDerivedFrom befree-2016 NP478002.RAm_PV2Zk2VDYJPoq29HkVUqpYL06DDNdCcal1hyl1DMk130_provenance.
- NP478002.RAm_PV2Zk2VDYJPoq29HkVUqpYL06DDNdCcal1hyl1DMk130_assertion wasGeneratedBy ECO_0000203 NP478002.RAm_PV2Zk2VDYJPoq29HkVUqpYL06DDNdCcal1hyl1DMk130_provenance.