Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP213913.RA3jKrFNrErRgP4-EDeJgPy7buVesNSOJ7THxflTYqJDo130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP213913.RA3jKrFNrErRgP4-EDeJgPy7buVesNSOJ7THxflTYqJDo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP213913.RA3jKrFNrErRgP4-EDeJgPy7buVesNSOJ7THxflTYqJDo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP213913.RA3jKrFNrErRgP4-EDeJgPy7buVesNSOJ7THxflTYqJDo130_provenance.
- NP213913.RA3jKrFNrErRgP4-EDeJgPy7buVesNSOJ7THxflTYqJDo130_assertion description "[it is reported for the first time that mutations in CABP4 lead to autosomal recessive congenital stationary night blindness]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP213913.RA3jKrFNrErRgP4-EDeJgPy7buVesNSOJ7THxflTYqJDo130_provenance.
- NP213913.RA3jKrFNrErRgP4-EDeJgPy7buVesNSOJ7THxflTYqJDo130_assertion evidence source_evidence_literature NP213913.RA3jKrFNrErRgP4-EDeJgPy7buVesNSOJ7THxflTYqJDo130_provenance.
- NP213913.RA3jKrFNrErRgP4-EDeJgPy7buVesNSOJ7THxflTYqJDo130_assertion SIO_000772 16960802 NP213913.RA3jKrFNrErRgP4-EDeJgPy7buVesNSOJ7THxflTYqJDo130_provenance.
- NP213913.RA3jKrFNrErRgP4-EDeJgPy7buVesNSOJ7THxflTYqJDo130_assertion wasDerivedFrom lhgdn-20090331 NP213913.RA3jKrFNrErRgP4-EDeJgPy7buVesNSOJ7THxflTYqJDo130_provenance.
- NP213913.RA3jKrFNrErRgP4-EDeJgPy7buVesNSOJ7THxflTYqJDo130_assertion wasGeneratedBy ECO_0000203 NP213913.RA3jKrFNrErRgP4-EDeJgPy7buVesNSOJ7THxflTYqJDo130_provenance.
- lhgdn-20090331 importedOn "2009-03-31" NP213913.RA3jKrFNrErRgP4-EDeJgPy7buVesNSOJ7THxflTYqJDo130_provenance.