Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP30667.RAPwD6wpJpZ1X7q985Ebs-xlr1aMR8QZ3_4aCYAOeFgBQ130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_curated type ECO_0000205 NP30667.RAPwD6wpJpZ1X7q985Ebs-xlr1aMR8QZ3_4aCYAOeFgBQ130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP30667.RAPwD6wpJpZ1X7q985Ebs-xlr1aMR8QZ3_4aCYAOeFgBQ130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP30667.RAPwD6wpJpZ1X7q985Ebs-xlr1aMR8QZ3_4aCYAOeFgBQ130_provenance.
- NP30667.RAPwD6wpJpZ1X7q985Ebs-xlr1aMR8QZ3_4aCYAOeFgBQ130_assertion description "[Germline gain-of-function mutations in RAF1 cause Noonan syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP30667.RAPwD6wpJpZ1X7q985Ebs-xlr1aMR8QZ3_4aCYAOeFgBQ130_provenance.
- NP30667.RAPwD6wpJpZ1X7q985Ebs-xlr1aMR8QZ3_4aCYAOeFgBQ130_assertion evidence source_evidence_curated NP30667.RAPwD6wpJpZ1X7q985Ebs-xlr1aMR8QZ3_4aCYAOeFgBQ130_provenance.
- NP30667.RAPwD6wpJpZ1X7q985Ebs-xlr1aMR8QZ3_4aCYAOeFgBQ130_assertion SIO_000772 17603482 NP30667.RAPwD6wpJpZ1X7q985Ebs-xlr1aMR8QZ3_4aCYAOeFgBQ130_provenance.
- NP30667.RAPwD6wpJpZ1X7q985Ebs-xlr1aMR8QZ3_4aCYAOeFgBQ130_assertion wasDerivedFrom ctd_human-20130708 NP30667.RAPwD6wpJpZ1X7q985Ebs-xlr1aMR8QZ3_4aCYAOeFgBQ130_provenance.
- NP30667.RAPwD6wpJpZ1X7q985Ebs-xlr1aMR8QZ3_4aCYAOeFgBQ130_assertion wasGeneratedBy ECO_0000218 NP30667.RAPwD6wpJpZ1X7q985Ebs-xlr1aMR8QZ3_4aCYAOeFgBQ130_provenance.
- ctd_human-20130708 importedOn "2013-07-24" NP30667.RAPwD6wpJpZ1X7q985Ebs-xlr1aMR8QZ3_4aCYAOeFgBQ130_provenance.