Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP26321.RAI8hjTcp7tiZAczB7nlpR5hm07M9FCbY_kSfSBjsd0Vo130_assertion> ?p ?o ?g. }
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- NP26321.RAI8hjTcp7tiZAczB7nlpR5hm07M9FCbY_kSfSBjsd0Vo130_assertion type Assertion NP26321.RAI8hjTcp7tiZAczB7nlpR5hm07M9FCbY_kSfSBjsd0Vo130_head.
- NP26321.RAI8hjTcp7tiZAczB7nlpR5hm07M9FCbY_kSfSBjsd0Vo130_assertion description "[Evidence for a recessive inheritance of Turcot's syndrome caused by compound heterozygous mutations within the PMS2 gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP26321.RAI8hjTcp7tiZAczB7nlpR5hm07M9FCbY_kSfSBjsd0Vo130_provenance.
- NP26321.RAI8hjTcp7tiZAczB7nlpR5hm07M9FCbY_kSfSBjsd0Vo130_assertion evidence source_evidence_curated NP26321.RAI8hjTcp7tiZAczB7nlpR5hm07M9FCbY_kSfSBjsd0Vo130_provenance.
- NP26321.RAI8hjTcp7tiZAczB7nlpR5hm07M9FCbY_kSfSBjsd0Vo130_assertion SIO_000772 10763829 NP26321.RAI8hjTcp7tiZAczB7nlpR5hm07M9FCbY_kSfSBjsd0Vo130_provenance.
- NP26321.RAI8hjTcp7tiZAczB7nlpR5hm07M9FCbY_kSfSBjsd0Vo130_assertion wasDerivedFrom ctd_human-20150221 NP26321.RAI8hjTcp7tiZAczB7nlpR5hm07M9FCbY_kSfSBjsd0Vo130_provenance.
- NP26321.RAI8hjTcp7tiZAczB7nlpR5hm07M9FCbY_kSfSBjsd0Vo130_assertion wasGeneratedBy ECO_0000218 NP26321.RAI8hjTcp7tiZAczB7nlpR5hm07M9FCbY_kSfSBjsd0Vo130_provenance.