Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1330674.RAHgm0sSPVREwYCxu-M2Dex1SNiI9qxrG5g74bi2KCN50130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP1330674.RAHgm0sSPVREwYCxu-M2Dex1SNiI9qxrG5g74bi2KCN50130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1330674.RAHgm0sSPVREwYCxu-M2Dex1SNiI9qxrG5g74bi2KCN50130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1330674.RAHgm0sSPVREwYCxu-M2Dex1SNiI9qxrG5g74bi2KCN50130_provenance.
- befree-2016 importedOn "2016-02-19" NP1330674.RAHgm0sSPVREwYCxu-M2Dex1SNiI9qxrG5g74bi2KCN50130_provenance.
- NP1330674.RAHgm0sSPVREwYCxu-M2Dex1SNiI9qxrG5g74bi2KCN50130_assertion wasGeneratedBy ECO_0000203 NP1330674.RAHgm0sSPVREwYCxu-M2Dex1SNiI9qxrG5g74bi2KCN50130_provenance.
- NP1330674.RAHgm0sSPVREwYCxu-M2Dex1SNiI9qxrG5g74bi2KCN50130_assertion wasDerivedFrom befree-2016 NP1330674.RAHgm0sSPVREwYCxu-M2Dex1SNiI9qxrG5g74bi2KCN50130_provenance.
- NP1330674.RAHgm0sSPVREwYCxu-M2Dex1SNiI9qxrG5g74bi2KCN50130_assertion SIO_000772 8045710 NP1330674.RAHgm0sSPVREwYCxu-M2Dex1SNiI9qxrG5g74bi2KCN50130_provenance.
- NP1330674.RAHgm0sSPVREwYCxu-M2Dex1SNiI9qxrG5g74bi2KCN50130_assertion evidence source_evidence_literature NP1330674.RAHgm0sSPVREwYCxu-M2Dex1SNiI9qxrG5g74bi2KCN50130_provenance.
- NP1330674.RAHgm0sSPVREwYCxu-M2Dex1SNiI9qxrG5g74bi2KCN50130_assertion description "[Patients from two families, one with a mutation in codon 167 (Gly167Asp) leading to macular degeneration and another with a mutation in codon 210 (Pro210Ser) leading to retinitis pigmentosa, were studied with clinical examinations and measurements of rod and cone sensitivities and dark adaptation, electroretinography, and rhodopsin levels.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1330674.RAHgm0sSPVREwYCxu-M2Dex1SNiI9qxrG5g74bi2KCN50130_provenance.