Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP218687.RAHqt-ylFfIXq4QOZiBDTehUkV0NvemYlZLKqiGYbbuhY130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP218687.RAHqt-ylFfIXq4QOZiBDTehUkV0NvemYlZLKqiGYbbuhY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP218687.RAHqt-ylFfIXq4QOZiBDTehUkV0NvemYlZLKqiGYbbuhY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP218687.RAHqt-ylFfIXq4QOZiBDTehUkV0NvemYlZLKqiGYbbuhY130_provenance.
- NP218687.RAHqt-ylFfIXq4QOZiBDTehUkV0NvemYlZLKqiGYbbuhY130_assertion description "[We identified 185 infants and children with homozygous or compound heterozygous ABCA3 mutations and lung disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP218687.RAHqt-ylFfIXq4QOZiBDTehUkV0NvemYlZLKqiGYbbuhY130_provenance.
- NP218687.RAHqt-ylFfIXq4QOZiBDTehUkV0NvemYlZLKqiGYbbuhY130_assertion evidence source_evidence_literature NP218687.RAHqt-ylFfIXq4QOZiBDTehUkV0NvemYlZLKqiGYbbuhY130_provenance.
- NP218687.RAHqt-ylFfIXq4QOZiBDTehUkV0NvemYlZLKqiGYbbuhY130_assertion SIO_000772 24871971 NP218687.RAHqt-ylFfIXq4QOZiBDTehUkV0NvemYlZLKqiGYbbuhY130_provenance.
- NP218687.RAHqt-ylFfIXq4QOZiBDTehUkV0NvemYlZLKqiGYbbuhY130_assertion wasDerivedFrom befree-20150227 NP218687.RAHqt-ylFfIXq4QOZiBDTehUkV0NvemYlZLKqiGYbbuhY130_provenance.
- NP218687.RAHqt-ylFfIXq4QOZiBDTehUkV0NvemYlZLKqiGYbbuhY130_assertion wasGeneratedBy ECO_0000203 NP218687.RAHqt-ylFfIXq4QOZiBDTehUkV0NvemYlZLKqiGYbbuhY130_provenance.
- befree-20150227 importedOn "2015-02-27" NP218687.RAHqt-ylFfIXq4QOZiBDTehUkV0NvemYlZLKqiGYbbuhY130_provenance.