Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP536688.RA7RixuGVCz16FRjpPwHiNFbj5aV6fZTK26cnGBVS0sx8130_assertion> ?p ?o ?g. }
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- NP536688.RA7RixuGVCz16FRjpPwHiNFbj5aV6fZTK26cnGBVS0sx8130_assertion type Assertion NP536688.RA7RixuGVCz16FRjpPwHiNFbj5aV6fZTK26cnGBVS0sx8130_head.
- NP536688.RA7RixuGVCz16FRjpPwHiNFbj5aV6fZTK26cnGBVS0sx8130_assertion wasGeneratedBy ECO_0000203 NP536688.RA7RixuGVCz16FRjpPwHiNFbj5aV6fZTK26cnGBVS0sx8130_provenance.
- NP536688.RA7RixuGVCz16FRjpPwHiNFbj5aV6fZTK26cnGBVS0sx8130_assertion wasDerivedFrom befree-20140225 NP536688.RA7RixuGVCz16FRjpPwHiNFbj5aV6fZTK26cnGBVS0sx8130_provenance.
- NP536688.RA7RixuGVCz16FRjpPwHiNFbj5aV6fZTK26cnGBVS0sx8130_assertion SIO_000772 21236492 NP536688.RA7RixuGVCz16FRjpPwHiNFbj5aV6fZTK26cnGBVS0sx8130_provenance.
- NP536688.RA7RixuGVCz16FRjpPwHiNFbj5aV6fZTK26cnGBVS0sx8130_assertion evidence source_evidence_literature NP536688.RA7RixuGVCz16FRjpPwHiNFbj5aV6fZTK26cnGBVS0sx8130_provenance.
- NP536688.RA7RixuGVCz16FRjpPwHiNFbj5aV6fZTK26cnGBVS0sx8130_assertion description "[A novel mutation of LAMB2 in a multigenerational mennonite family reveals a new phenotypic variant of Pierson syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP536688.RA7RixuGVCz16FRjpPwHiNFbj5aV6fZTK26cnGBVS0sx8130_provenance.