Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP556873.RABwMltYbRRUirtqHz3mx4IRs4Mwvta4H5LVIWIf5Nv4g130_assertion> ?p ?o ?g. }
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- NP556873.RABwMltYbRRUirtqHz3mx4IRs4Mwvta4H5LVIWIf5Nv4g130_assertion type Assertion NP556873.RABwMltYbRRUirtqHz3mx4IRs4Mwvta4H5LVIWIf5Nv4g130_head.
- NP556873.RABwMltYbRRUirtqHz3mx4IRs4Mwvta4H5LVIWIf5Nv4g130_assertion wasGeneratedBy ECO_0000203 NP556873.RABwMltYbRRUirtqHz3mx4IRs4Mwvta4H5LVIWIf5Nv4g130_provenance.
- NP556873.RABwMltYbRRUirtqHz3mx4IRs4Mwvta4H5LVIWIf5Nv4g130_assertion wasDerivedFrom befree-20150227 NP556873.RABwMltYbRRUirtqHz3mx4IRs4Mwvta4H5LVIWIf5Nv4g130_provenance.
- NP556873.RABwMltYbRRUirtqHz3mx4IRs4Mwvta4H5LVIWIf5Nv4g130_assertion SIO_000772 24405844 NP556873.RABwMltYbRRUirtqHz3mx4IRs4Mwvta4H5LVIWIf5Nv4g130_provenance.
- NP556873.RABwMltYbRRUirtqHz3mx4IRs4Mwvta4H5LVIWIf5Nv4g130_assertion evidence source_evidence_literature NP556873.RABwMltYbRRUirtqHz3mx4IRs4Mwvta4H5LVIWIf5Nv4g130_provenance.
- NP556873.RABwMltYbRRUirtqHz3mx4IRs4Mwvta4H5LVIWIf5Nv4g130_assertion description "[A novel MIP gene mutation associated with autosomal dominant congenital cataracts in a Chinese family.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP556873.RABwMltYbRRUirtqHz3mx4IRs4Mwvta4H5LVIWIf5Nv4g130_provenance.