Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP547253.RAg1xm95zdXJvlbjZam7qquwVKTYjpGUjSZcqZDSCrcR0130_assertion> ?p ?o ?g. }
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- NP547253.RAg1xm95zdXJvlbjZam7qquwVKTYjpGUjSZcqZDSCrcR0130_assertion type Assertion NP547253.RAg1xm95zdXJvlbjZam7qquwVKTYjpGUjSZcqZDSCrcR0130_head.
- NP547253.RAg1xm95zdXJvlbjZam7qquwVKTYjpGUjSZcqZDSCrcR0130_assertion description "[In summary, biallelic germline mutations of MYH are unlikely to cause colorectal cancer in patients sharing clinical features with hereditary nonpolyposis colorectal cancer families without mismatch repair defect and therefore cannot fill the molecular diagnostic gap in this subgroup of Bethesda-positive patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP547253.RAg1xm95zdXJvlbjZam7qquwVKTYjpGUjSZcqZDSCrcR0130_provenance.
- NP547253.RAg1xm95zdXJvlbjZam7qquwVKTYjpGUjSZcqZDSCrcR0130_assertion evidence source_evidence_literature NP547253.RAg1xm95zdXJvlbjZam7qquwVKTYjpGUjSZcqZDSCrcR0130_provenance.
- NP547253.RAg1xm95zdXJvlbjZam7qquwVKTYjpGUjSZcqZDSCrcR0130_assertion SIO_000772 16645203 NP547253.RAg1xm95zdXJvlbjZam7qquwVKTYjpGUjSZcqZDSCrcR0130_provenance.
- NP547253.RAg1xm95zdXJvlbjZam7qquwVKTYjpGUjSZcqZDSCrcR0130_assertion wasDerivedFrom befree-2016 NP547253.RAg1xm95zdXJvlbjZam7qquwVKTYjpGUjSZcqZDSCrcR0130_provenance.
- NP547253.RAg1xm95zdXJvlbjZam7qquwVKTYjpGUjSZcqZDSCrcR0130_assertion wasGeneratedBy ECO_0000203 NP547253.RAg1xm95zdXJvlbjZam7qquwVKTYjpGUjSZcqZDSCrcR0130_provenance.