Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1246837.RA3zVoNmhSM2kfhukB_Hp-qUXnMMlUF6eNoe6A9OHbHB8130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP1246837.RA3zVoNmhSM2kfhukB_Hp-qUXnMMlUF6eNoe6A9OHbHB8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1246837.RA3zVoNmhSM2kfhukB_Hp-qUXnMMlUF6eNoe6A9OHbHB8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1246837.RA3zVoNmhSM2kfhukB_Hp-qUXnMMlUF6eNoe6A9OHbHB8130_provenance.
- NP1246837.RA3zVoNmhSM2kfhukB_Hp-qUXnMMlUF6eNoe6A9OHbHB8130_assertion description "[Transgenic mouse studies have indicated that all codon 129 genotypes are susceptible to vCJD and that genotype may influence whether disease appears in a clinical or asymptomatic form, supported by the appearance of the first case of potential asymptomatic vCJD infection in a PRNP 129MV patient.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1246837.RA3zVoNmhSM2kfhukB_Hp-qUXnMMlUF6eNoe6A9OHbHB8130_provenance.
- NP1246837.RA3zVoNmhSM2kfhukB_Hp-qUXnMMlUF6eNoe6A9OHbHB8130_assertion evidence source_evidence_literature NP1246837.RA3zVoNmhSM2kfhukB_Hp-qUXnMMlUF6eNoe6A9OHbHB8130_provenance.
- NP1246837.RA3zVoNmhSM2kfhukB_Hp-qUXnMMlUF6eNoe6A9OHbHB8130_assertion SIO_000772 25495404 NP1246837.RA3zVoNmhSM2kfhukB_Hp-qUXnMMlUF6eNoe6A9OHbHB8130_provenance.
- NP1246837.RA3zVoNmhSM2kfhukB_Hp-qUXnMMlUF6eNoe6A9OHbHB8130_assertion wasDerivedFrom befree-2016 NP1246837.RA3zVoNmhSM2kfhukB_Hp-qUXnMMlUF6eNoe6A9OHbHB8130_provenance.
- NP1246837.RA3zVoNmhSM2kfhukB_Hp-qUXnMMlUF6eNoe6A9OHbHB8130_assertion wasGeneratedBy ECO_0000203 NP1246837.RA3zVoNmhSM2kfhukB_Hp-qUXnMMlUF6eNoe6A9OHbHB8130_provenance.
- befree-2016 importedOn "2016-02-19" NP1246837.RA3zVoNmhSM2kfhukB_Hp-qUXnMMlUF6eNoe6A9OHbHB8130_provenance.