Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP406416.RAr9hZ59uP7yCztYNFLV5cVzf3QYbs15ZoT68A0WNnep4130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP406416.RAr9hZ59uP7yCztYNFLV5cVzf3QYbs15ZoT68A0WNnep4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP406416.RAr9hZ59uP7yCztYNFLV5cVzf3QYbs15ZoT68A0WNnep4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP406416.RAr9hZ59uP7yCztYNFLV5cVzf3QYbs15ZoT68A0WNnep4130_provenance.
- NP406416.RAr9hZ59uP7yCztYNFLV5cVzf3QYbs15ZoT68A0WNnep4130_assertion wasGeneratedBy ECO_0000203 NP406416.RAr9hZ59uP7yCztYNFLV5cVzf3QYbs15ZoT68A0WNnep4130_provenance.
- NP406416.RAr9hZ59uP7yCztYNFLV5cVzf3QYbs15ZoT68A0WNnep4130_assertion wasDerivedFrom befree-20140225 NP406416.RAr9hZ59uP7yCztYNFLV5cVzf3QYbs15ZoT68A0WNnep4130_provenance.
- NP406416.RAr9hZ59uP7yCztYNFLV5cVzf3QYbs15ZoT68A0WNnep4130_assertion SIO_000772 17044635 NP406416.RAr9hZ59uP7yCztYNFLV5cVzf3QYbs15ZoT68A0WNnep4130_provenance.
- NP406416.RAr9hZ59uP7yCztYNFLV5cVzf3QYbs15ZoT68A0WNnep4130_assertion evidence source_evidence_literature NP406416.RAr9hZ59uP7yCztYNFLV5cVzf3QYbs15ZoT68A0WNnep4130_provenance.
- NP406416.RAr9hZ59uP7yCztYNFLV5cVzf3QYbs15ZoT68A0WNnep4130_assertion description "[This rare variant of IPF has an autosomal dominant mode of inheritance with variable expressivity, and is commonly associated with a mutation of the surfactant protein C gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP406416.RAr9hZ59uP7yCztYNFLV5cVzf3QYbs15ZoT68A0WNnep4130_provenance.
- befree-20140225 importedOn "2014-02-25" NP406416.RAr9hZ59uP7yCztYNFLV5cVzf3QYbs15ZoT68A0WNnep4130_provenance.