Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP223957.RA5PFwKFwWBEeVKFSzy9VdD5qJeBp_UCXFpOW4KVFsnF0130_assertion> ?p ?o ?g. }
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- NP223957.RA5PFwKFwWBEeVKFSzy9VdD5qJeBp_UCXFpOW4KVFsnF0130_assertion type Assertion NP223957.RA5PFwKFwWBEeVKFSzy9VdD5qJeBp_UCXFpOW4KVFsnF0130_head.
- NP223957.RA5PFwKFwWBEeVKFSzy9VdD5qJeBp_UCXFpOW4KVFsnF0130_assertion description "[Germline NF1, c-RET, SDH, and VHL mutations cause familial pheochromocytoma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP223957.RA5PFwKFwWBEeVKFSzy9VdD5qJeBp_UCXFpOW4KVFsnF0130_provenance.
- NP223957.RA5PFwKFwWBEeVKFSzy9VdD5qJeBp_UCXFpOW4KVFsnF0130_assertion evidence source_evidence_literature NP223957.RA5PFwKFwWBEeVKFSzy9VdD5qJeBp_UCXFpOW4KVFsnF0130_provenance.
- NP223957.RA5PFwKFwWBEeVKFSzy9VdD5qJeBp_UCXFpOW4KVFsnF0130_assertion SIO_000772 16098468 NP223957.RA5PFwKFwWBEeVKFSzy9VdD5qJeBp_UCXFpOW4KVFsnF0130_provenance.
- NP223957.RA5PFwKFwWBEeVKFSzy9VdD5qJeBp_UCXFpOW4KVFsnF0130_assertion wasDerivedFrom befree-20140225 NP223957.RA5PFwKFwWBEeVKFSzy9VdD5qJeBp_UCXFpOW4KVFsnF0130_provenance.
- NP223957.RA5PFwKFwWBEeVKFSzy9VdD5qJeBp_UCXFpOW4KVFsnF0130_assertion wasGeneratedBy ECO_0000203 NP223957.RA5PFwKFwWBEeVKFSzy9VdD5qJeBp_UCXFpOW4KVFsnF0130_provenance.