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- NP320189.RA-FJdq80PZv-bXUu3LHR3A_y8TPf4eN2_aTMRbW5tLh8130_assertion type Assertion NP320189.RA-FJdq80PZv-bXUu3LHR3A_y8TPf4eN2_aTMRbW5tLh8130_head.
- NP320189.RA-FJdq80PZv-bXUu3LHR3A_y8TPf4eN2_aTMRbW5tLh8130_assertion wasGeneratedBy ECO_0000203 NP320189.RA-FJdq80PZv-bXUu3LHR3A_y8TPf4eN2_aTMRbW5tLh8130_provenance.
- NP320189.RA-FJdq80PZv-bXUu3LHR3A_y8TPf4eN2_aTMRbW5tLh8130_assertion wasDerivedFrom befree-20150227 NP320189.RA-FJdq80PZv-bXUu3LHR3A_y8TPf4eN2_aTMRbW5tLh8130_provenance.
- NP320189.RA-FJdq80PZv-bXUu3LHR3A_y8TPf4eN2_aTMRbW5tLh8130_assertion SIO_000772 23714752 NP320189.RA-FJdq80PZv-bXUu3LHR3A_y8TPf4eN2_aTMRbW5tLh8130_provenance.
- NP320189.RA-FJdq80PZv-bXUu3LHR3A_y8TPf4eN2_aTMRbW5tLh8130_assertion evidence source_evidence_literature NP320189.RA-FJdq80PZv-bXUu3LHR3A_y8TPf4eN2_aTMRbW5tLh8130_provenance.
- NP320189.RA-FJdq80PZv-bXUu3LHR3A_y8TPf4eN2_aTMRbW5tLh8130_assertion description "[Whereas mutations in COL4A5 and contiguous X-chromosomal deletions involving COL4A5 and COL4A6 are associated with X-linked Alport syndrome, a nephropathy associated with deafness and cataract, mutations in COL4A6 alone have not been related to any hereditary disease so far.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP320189.RA-FJdq80PZv-bXUu3LHR3A_y8TPf4eN2_aTMRbW5tLh8130_provenance.