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- NP678269.RASGbcnoIUVwCAMv2-awPdplNUexqBgnZIl4PTDO9Gs1Q130_assertion type Assertion NP678269.RASGbcnoIUVwCAMv2-awPdplNUexqBgnZIl4PTDO9Gs1Q130_head.
- NP678269.RASGbcnoIUVwCAMv2-awPdplNUexqBgnZIl4PTDO9Gs1Q130_assertion wasGeneratedBy ECO_0000203 NP678269.RASGbcnoIUVwCAMv2-awPdplNUexqBgnZIl4PTDO9Gs1Q130_provenance.
- NP678269.RASGbcnoIUVwCAMv2-awPdplNUexqBgnZIl4PTDO9Gs1Q130_assertion wasDerivedFrom befree-20140225 NP678269.RASGbcnoIUVwCAMv2-awPdplNUexqBgnZIl4PTDO9Gs1Q130_provenance.
- NP678269.RASGbcnoIUVwCAMv2-awPdplNUexqBgnZIl4PTDO9Gs1Q130_assertion SIO_000772 16000562 NP678269.RASGbcnoIUVwCAMv2-awPdplNUexqBgnZIl4PTDO9Gs1Q130_provenance.
- NP678269.RASGbcnoIUVwCAMv2-awPdplNUexqBgnZIl4PTDO9Gs1Q130_assertion evidence source_evidence_literature NP678269.RASGbcnoIUVwCAMv2-awPdplNUexqBgnZIl4PTDO9Gs1Q130_provenance.
- NP678269.RASGbcnoIUVwCAMv2-awPdplNUexqBgnZIl4PTDO9Gs1Q130_assertion description "[Our findings support a role for MSH6 in Turcot syndrome and are consistent with an autosomal recessive mode of inheritance.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP678269.RASGbcnoIUVwCAMv2-awPdplNUexqBgnZIl4PTDO9Gs1Q130_provenance.