Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1380134.RAATEloVYZW3OYeXk4558VfW0-yb6txmFnE74ODWhi4VE130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP1380134.RAATEloVYZW3OYeXk4558VfW0-yb6txmFnE74ODWhi4VE130_assertion type Assertion NP1380134.RAATEloVYZW3OYeXk4558VfW0-yb6txmFnE74ODWhi4VE130_head.
- NP1380134.RAATEloVYZW3OYeXk4558VfW0-yb6txmFnE74ODWhi4VE130_assertion description "[The HNPCC phenotype has been shown to segregate with germline mutations in the human homologues of the DNA mismatch repair genes MSH2, MLH1, PMS1, and PMS2.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1380134.RAATEloVYZW3OYeXk4558VfW0-yb6txmFnE74ODWhi4VE130_provenance.
- NP1380134.RAATEloVYZW3OYeXk4558VfW0-yb6txmFnE74ODWhi4VE130_assertion evidence source_evidence_literature NP1380134.RAATEloVYZW3OYeXk4558VfW0-yb6txmFnE74ODWhi4VE130_provenance.
- NP1380134.RAATEloVYZW3OYeXk4558VfW0-yb6txmFnE74ODWhi4VE130_assertion SIO_000772 9288790 NP1380134.RAATEloVYZW3OYeXk4558VfW0-yb6txmFnE74ODWhi4VE130_provenance.
- NP1380134.RAATEloVYZW3OYeXk4558VfW0-yb6txmFnE74ODWhi4VE130_assertion wasDerivedFrom befree-2016 NP1380134.RAATEloVYZW3OYeXk4558VfW0-yb6txmFnE74ODWhi4VE130_provenance.
- NP1380134.RAATEloVYZW3OYeXk4558VfW0-yb6txmFnE74ODWhi4VE130_assertion wasGeneratedBy ECO_0000203 NP1380134.RAATEloVYZW3OYeXk4558VfW0-yb6txmFnE74ODWhi4VE130_provenance.