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- source_evidence_literature type ECO_0000212 NP1238863.RA6XotCNsmk3GMB1agN8_VBxZpHTN4jsWhwV61MLvMU-4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1238863.RA6XotCNsmk3GMB1agN8_VBxZpHTN4jsWhwV61MLvMU-4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1238863.RA6XotCNsmk3GMB1agN8_VBxZpHTN4jsWhwV61MLvMU-4130_provenance.
- 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.
- befree-2016 importedOn "2016-02-19" NP1238863.RA6XotCNsmk3GMB1agN8_VBxZpHTN4jsWhwV61MLvMU-4130_provenance.