Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1238863.RA6XotCNsmk3GMB1agN8_VBxZpHTN4jsWhwV61MLvMU-4130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP1238863.RA6XotCNsmk3GMB1agN8_VBxZpHTN4jsWhwV61MLvMU-4130_assertion type Assertion NP1238863.RA6XotCNsmk3GMB1agN8_VBxZpHTN4jsWhwV61MLvMU-4130_head.
- NP1238863.RA6XotCNsmk3GMB1agN8_VBxZpHTN4jsWhwV61MLvMU-4130_assertion description "[To understand the molecular basis of the genetic defect, the gene encoding cystatin C was isolated from genomic DNA libraries made from normal tissue and the brain of an Icelandic patient with hereditary cerebral hemorrhage with amyloidosis (HCHWA-I).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1238863.RA6XotCNsmk3GMB1agN8_VBxZpHTN4jsWhwV61MLvMU-4130_provenance.
- NP1238863.RA6XotCNsmk3GMB1agN8_VBxZpHTN4jsWhwV61MLvMU-4130_assertion evidence source_evidence_literature NP1238863.RA6XotCNsmk3GMB1agN8_VBxZpHTN4jsWhwV61MLvMU-4130_provenance.
- NP1238863.RA6XotCNsmk3GMB1agN8_VBxZpHTN4jsWhwV61MLvMU-4130_assertion SIO_000772 2541223 NP1238863.RA6XotCNsmk3GMB1agN8_VBxZpHTN4jsWhwV61MLvMU-4130_provenance.
- NP1238863.RA6XotCNsmk3GMB1agN8_VBxZpHTN4jsWhwV61MLvMU-4130_assertion wasDerivedFrom befree-2016 NP1238863.RA6XotCNsmk3GMB1agN8_VBxZpHTN4jsWhwV61MLvMU-4130_provenance.
- NP1238863.RA6XotCNsmk3GMB1agN8_VBxZpHTN4jsWhwV61MLvMU-4130_assertion wasGeneratedBy ECO_0000203 NP1238863.RA6XotCNsmk3GMB1agN8_VBxZpHTN4jsWhwV61MLvMU-4130_provenance.