Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1211632.RALP7SFzwsVzFZDHyLJiFF8wUQfhw4xGa9pNEcrStGC8M130_assertion> ?p ?o ?g. }
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- NP1211632.RALP7SFzwsVzFZDHyLJiFF8wUQfhw4xGa9pNEcrStGC8M130_assertion type Assertion NP1211632.RALP7SFzwsVzFZDHyLJiFF8wUQfhw4xGa9pNEcrStGC8M130_head.
- NP1211632.RALP7SFzwsVzFZDHyLJiFF8wUQfhw4xGa9pNEcrStGC8M130_assertion description "[Lynch syndrome is the most common form of hereditary colorectal cancer and is caused by germline mutations in the mismatch repair (MMR) genes MLH1, MSH2, MSH6 and PMS2.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1211632.RALP7SFzwsVzFZDHyLJiFF8wUQfhw4xGa9pNEcrStGC8M130_provenance.
- NP1211632.RALP7SFzwsVzFZDHyLJiFF8wUQfhw4xGa9pNEcrStGC8M130_assertion evidence source_evidence_literature NP1211632.RALP7SFzwsVzFZDHyLJiFF8wUQfhw4xGa9pNEcrStGC8M130_provenance.
- NP1211632.RALP7SFzwsVzFZDHyLJiFF8wUQfhw4xGa9pNEcrStGC8M130_assertion SIO_000772 25133505 NP1211632.RALP7SFzwsVzFZDHyLJiFF8wUQfhw4xGa9pNEcrStGC8M130_provenance.
- NP1211632.RALP7SFzwsVzFZDHyLJiFF8wUQfhw4xGa9pNEcrStGC8M130_assertion wasDerivedFrom befree-2016 NP1211632.RALP7SFzwsVzFZDHyLJiFF8wUQfhw4xGa9pNEcrStGC8M130_provenance.
- NP1211632.RALP7SFzwsVzFZDHyLJiFF8wUQfhw4xGa9pNEcrStGC8M130_assertion wasGeneratedBy ECO_0000203 NP1211632.RALP7SFzwsVzFZDHyLJiFF8wUQfhw4xGa9pNEcrStGC8M130_provenance.