Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP761076.RAFxMXN4CKEiLxDaf5TFozX1EkHe1_C81K3lwcngJVkPs130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP761076.RAFxMXN4CKEiLxDaf5TFozX1EkHe1_C81K3lwcngJVkPs130_assertion type Assertion NP761076.RAFxMXN4CKEiLxDaf5TFozX1EkHe1_C81K3lwcngJVkPs130_head.
- NP761076.RAFxMXN4CKEiLxDaf5TFozX1EkHe1_C81K3lwcngJVkPs130_assertion wasGeneratedBy ECO_0000203 NP761076.RAFxMXN4CKEiLxDaf5TFozX1EkHe1_C81K3lwcngJVkPs130_provenance.
- NP761076.RAFxMXN4CKEiLxDaf5TFozX1EkHe1_C81K3lwcngJVkPs130_assertion wasDerivedFrom befree-2016 NP761076.RAFxMXN4CKEiLxDaf5TFozX1EkHe1_C81K3lwcngJVkPs130_provenance.
- NP761076.RAFxMXN4CKEiLxDaf5TFozX1EkHe1_C81K3lwcngJVkPs130_assertion SIO_000772 19728162 NP761076.RAFxMXN4CKEiLxDaf5TFozX1EkHe1_C81K3lwcngJVkPs130_provenance.
- NP761076.RAFxMXN4CKEiLxDaf5TFozX1EkHe1_C81K3lwcngJVkPs130_assertion evidence source_evidence_literature NP761076.RAFxMXN4CKEiLxDaf5TFozX1EkHe1_C81K3lwcngJVkPs130_provenance.
- NP761076.RAFxMXN4CKEiLxDaf5TFozX1EkHe1_C81K3lwcngJVkPs130_assertion description "[Lynch syndrome is an inherited cancer syndrome caused by germline mutations in mismatch repair (MMR) genes MLH1, MSH2, MSH6 and PMS2.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP761076.RAFxMXN4CKEiLxDaf5TFozX1EkHe1_C81K3lwcngJVkPs130_provenance.