Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP52033.RA1y0wa4I4u-kj3_mOIexjmoH6Fkzif9hArnhe49Ee5_k130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP52033.RA1y0wa4I4u-kj3_mOIexjmoH6Fkzif9hArnhe49Ee5_k130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP52033.RA1y0wa4I4u-kj3_mOIexjmoH6Fkzif9hArnhe49Ee5_k130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP52033.RA1y0wa4I4u-kj3_mOIexjmoH6Fkzif9hArnhe49Ee5_k130_provenance.
- NP52033.RA1y0wa4I4u-kj3_mOIexjmoH6Fkzif9hArnhe49Ee5_k130_assertion description "[The results of our study suggest that mutations in HNF3B are not a common cause of MODY in Japanese subjects.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP52033.RA1y0wa4I4u-kj3_mOIexjmoH6Fkzif9hArnhe49Ee5_k130_provenance.
- NP52033.RA1y0wa4I4u-kj3_mOIexjmoH6Fkzif9hArnhe49Ee5_k130_assertion evidence source_evidence_literature NP52033.RA1y0wa4I4u-kj3_mOIexjmoH6Fkzif9hArnhe49Ee5_k130_provenance.
- NP52033.RA1y0wa4I4u-kj3_mOIexjmoH6Fkzif9hArnhe49Ee5_k130_assertion SIO_000772 10868948 NP52033.RA1y0wa4I4u-kj3_mOIexjmoH6Fkzif9hArnhe49Ee5_k130_provenance.
- NP52033.RA1y0wa4I4u-kj3_mOIexjmoH6Fkzif9hArnhe49Ee5_k130_assertion wasDerivedFrom gad-20150221 NP52033.RA1y0wa4I4u-kj3_mOIexjmoH6Fkzif9hArnhe49Ee5_k130_provenance.
- NP52033.RA1y0wa4I4u-kj3_mOIexjmoH6Fkzif9hArnhe49Ee5_k130_assertion wasGeneratedBy ECO_0000203 NP52033.RA1y0wa4I4u-kj3_mOIexjmoH6Fkzif9hArnhe49Ee5_k130_provenance.
- gad-20150221 importedOn "2015-02-21" NP52033.RA1y0wa4I4u-kj3_mOIexjmoH6Fkzif9hArnhe49Ee5_k130_provenance.