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- source_evidence_literature type ECO_0000212 NP1380134.RAATEloVYZW3OYeXk4558VfW0-yb6txmFnE74ODWhi4VE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1380134.RAATEloVYZW3OYeXk4558VfW0-yb6txmFnE74ODWhi4VE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1380134.RAATEloVYZW3OYeXk4558VfW0-yb6txmFnE74ODWhi4VE130_provenance.
- 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.
- befree-2016 importedOn "2016-02-19" NP1380134.RAATEloVYZW3OYeXk4558VfW0-yb6txmFnE74ODWhi4VE130_provenance.