Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP769587.RAV7G6kK-W0wOY3UhVvdrtFpbVf4IGQNaowDmAm_8ASac130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP769587.RAV7G6kK-W0wOY3UhVvdrtFpbVf4IGQNaowDmAm_8ASac130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP769587.RAV7G6kK-W0wOY3UhVvdrtFpbVf4IGQNaowDmAm_8ASac130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP769587.RAV7G6kK-W0wOY3UhVvdrtFpbVf4IGQNaowDmAm_8ASac130_provenance.
- NP769587.RAV7G6kK-W0wOY3UhVvdrtFpbVf4IGQNaowDmAm_8ASac130_assertion description "[Seventy percent of the cases of hereditary surfactant protein-B deficiency are caused by homozygosity for the 121ins2 mutation in the surfactant protein-B gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP769587.RAV7G6kK-W0wOY3UhVvdrtFpbVf4IGQNaowDmAm_8ASac130_provenance.
- NP769587.RAV7G6kK-W0wOY3UhVvdrtFpbVf4IGQNaowDmAm_8ASac130_assertion evidence source_evidence_literature NP769587.RAV7G6kK-W0wOY3UhVvdrtFpbVf4IGQNaowDmAm_8ASac130_provenance.
- NP769587.RAV7G6kK-W0wOY3UhVvdrtFpbVf4IGQNaowDmAm_8ASac130_assertion SIO_000772 19833825 NP769587.RAV7G6kK-W0wOY3UhVvdrtFpbVf4IGQNaowDmAm_8ASac130_provenance.
- NP769587.RAV7G6kK-W0wOY3UhVvdrtFpbVf4IGQNaowDmAm_8ASac130_assertion wasDerivedFrom befree-2016 NP769587.RAV7G6kK-W0wOY3UhVvdrtFpbVf4IGQNaowDmAm_8ASac130_provenance.
- NP769587.RAV7G6kK-W0wOY3UhVvdrtFpbVf4IGQNaowDmAm_8ASac130_assertion wasGeneratedBy ECO_0000203 NP769587.RAV7G6kK-W0wOY3UhVvdrtFpbVf4IGQNaowDmAm_8ASac130_provenance.
- befree-2016 importedOn "2016-02-19" NP769587.RAV7G6kK-W0wOY3UhVvdrtFpbVf4IGQNaowDmAm_8ASac130_provenance.