Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP798444.RATG598FKafr8lHSZV4BWk9u7g6bAM_2R_h3mqWjZgu0o130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP798444.RATG598FKafr8lHSZV4BWk9u7g6bAM_2R_h3mqWjZgu0o130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP798444.RATG598FKafr8lHSZV4BWk9u7g6bAM_2R_h3mqWjZgu0o130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP798444.RATG598FKafr8lHSZV4BWk9u7g6bAM_2R_h3mqWjZgu0o130_provenance.
- NP798444.RATG598FKafr8lHSZV4BWk9u7g6bAM_2R_h3mqWjZgu0o130_assertion description "[Studies of families with Birt-Hogg-Dub� syndrome (BHD) have recently revealed protein-truncating mutations in the BHD gene, leading to tumorigenesis of the skin and of different cell types of kidney.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP798444.RATG598FKafr8lHSZV4BWk9u7g6bAM_2R_h3mqWjZgu0o130_provenance.
- NP798444.RATG598FKafr8lHSZV4BWk9u7g6bAM_2R_h3mqWjZgu0o130_assertion evidence source_evidence_literature NP798444.RATG598FKafr8lHSZV4BWk9u7g6bAM_2R_h3mqWjZgu0o130_provenance.
- NP798444.RATG598FKafr8lHSZV4BWk9u7g6bAM_2R_h3mqWjZgu0o130_assertion SIO_000772 12907635 NP798444.RATG598FKafr8lHSZV4BWk9u7g6bAM_2R_h3mqWjZgu0o130_provenance.
- NP798444.RATG598FKafr8lHSZV4BWk9u7g6bAM_2R_h3mqWjZgu0o130_assertion wasDerivedFrom befree-20140225 NP798444.RATG598FKafr8lHSZV4BWk9u7g6bAM_2R_h3mqWjZgu0o130_provenance.
- NP798444.RATG598FKafr8lHSZV4BWk9u7g6bAM_2R_h3mqWjZgu0o130_assertion wasGeneratedBy ECO_0000203 NP798444.RATG598FKafr8lHSZV4BWk9u7g6bAM_2R_h3mqWjZgu0o130_provenance.
- befree-20140225 importedOn "2014-02-25" NP798444.RATG598FKafr8lHSZV4BWk9u7g6bAM_2R_h3mqWjZgu0o130_provenance.