Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP416060.RAkyluzDCbMmE45R2Sp_h9tdyPnzImUruKsgIAZDJS2PM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP416060.RAkyluzDCbMmE45R2Sp_h9tdyPnzImUruKsgIAZDJS2PM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP416060.RAkyluzDCbMmE45R2Sp_h9tdyPnzImUruKsgIAZDJS2PM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP416060.RAkyluzDCbMmE45R2Sp_h9tdyPnzImUruKsgIAZDJS2PM130_provenance.
- NP416060.RAkyluzDCbMmE45R2Sp_h9tdyPnzImUruKsgIAZDJS2PM130_assertion description "[Compound SFTPB 1549C-->GAA (121ins2) and 457delC heterozygosity in severe congenital lung disease and surfactant protein B (SP-B) deficiency.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP416060.RAkyluzDCbMmE45R2Sp_h9tdyPnzImUruKsgIAZDJS2PM130_provenance.
- NP416060.RAkyluzDCbMmE45R2Sp_h9tdyPnzImUruKsgIAZDJS2PM130_assertion evidence source_evidence_literature NP416060.RAkyluzDCbMmE45R2Sp_h9tdyPnzImUruKsgIAZDJS2PM130_provenance.
- NP416060.RAkyluzDCbMmE45R2Sp_h9tdyPnzImUruKsgIAZDJS2PM130_assertion SIO_000772 10571948 NP416060.RAkyluzDCbMmE45R2Sp_h9tdyPnzImUruKsgIAZDJS2PM130_provenance.
- NP416060.RAkyluzDCbMmE45R2Sp_h9tdyPnzImUruKsgIAZDJS2PM130_assertion wasDerivedFrom befree-20150227 NP416060.RAkyluzDCbMmE45R2Sp_h9tdyPnzImUruKsgIAZDJS2PM130_provenance.
- NP416060.RAkyluzDCbMmE45R2Sp_h9tdyPnzImUruKsgIAZDJS2PM130_assertion wasGeneratedBy ECO_0000203 NP416060.RAkyluzDCbMmE45R2Sp_h9tdyPnzImUruKsgIAZDJS2PM130_provenance.
- befree-20150227 importedOn "2015-02-27" NP416060.RAkyluzDCbMmE45R2Sp_h9tdyPnzImUruKsgIAZDJS2PM130_provenance.