Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP365516.RA8GF2WXF-m238YFZReCwvQzzFXQKK6wXvFUcpS30Bv1M130_assertion> ?p ?o ?g. }
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- NP365516.RA8GF2WXF-m238YFZReCwvQzzFXQKK6wXvFUcpS30Bv1M130_assertion type Assertion NP365516.RA8GF2WXF-m238YFZReCwvQzzFXQKK6wXvFUcpS30Bv1M130_head.
- NP365516.RA8GF2WXF-m238YFZReCwvQzzFXQKK6wXvFUcpS30Bv1M130_assertion wasGeneratedBy ECO_0000203 NP365516.RA8GF2WXF-m238YFZReCwvQzzFXQKK6wXvFUcpS30Bv1M130_provenance.
- NP365516.RA8GF2WXF-m238YFZReCwvQzzFXQKK6wXvFUcpS30Bv1M130_assertion wasDerivedFrom befree-20140225 NP365516.RA8GF2WXF-m238YFZReCwvQzzFXQKK6wXvFUcpS30Bv1M130_provenance.
- NP365516.RA8GF2WXF-m238YFZReCwvQzzFXQKK6wXvFUcpS30Bv1M130_assertion SIO_000772 10561721 NP365516.RA8GF2WXF-m238YFZReCwvQzzFXQKK6wXvFUcpS30Bv1M130_provenance.
- NP365516.RA8GF2WXF-m238YFZReCwvQzzFXQKK6wXvFUcpS30Bv1M130_assertion evidence source_evidence_literature NP365516.RA8GF2WXF-m238YFZReCwvQzzFXQKK6wXvFUcpS30Bv1M130_provenance.
- NP365516.RA8GF2WXF-m238YFZReCwvQzzFXQKK6wXvFUcpS30Bv1M130_assertion description "[The mutations in the helix initiation motif of K13 are the cause of WSN in these families.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP365516.RA8GF2WXF-m238YFZReCwvQzzFXQKK6wXvFUcpS30Bv1M130_provenance.