Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP860043.RA8HvaaiwH7FNrK4JVywBMSyKiBqBRTTAhwc6JgnGXU8g130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP860043.RA8HvaaiwH7FNrK4JVywBMSyKiBqBRTTAhwc6JgnGXU8g130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP860043.RA8HvaaiwH7FNrK4JVywBMSyKiBqBRTTAhwc6JgnGXU8g130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP860043.RA8HvaaiwH7FNrK4JVywBMSyKiBqBRTTAhwc6JgnGXU8g130_provenance.
- NP860043.RA8HvaaiwH7FNrK4JVywBMSyKiBqBRTTAhwc6JgnGXU8g130_assertion description "[HNF1 alpha gene coding regions mutations screening, in a Caucasian population clinically characterized as MODY from Argentina.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP860043.RA8HvaaiwH7FNrK4JVywBMSyKiBqBRTTAhwc6JgnGXU8g130_provenance.
- NP860043.RA8HvaaiwH7FNrK4JVywBMSyKiBqBRTTAhwc6JgnGXU8g130_assertion evidence source_evidence_literature NP860043.RA8HvaaiwH7FNrK4JVywBMSyKiBqBRTTAhwc6JgnGXU8g130_provenance.
- NP860043.RA8HvaaiwH7FNrK4JVywBMSyKiBqBRTTAhwc6JgnGXU8g130_assertion SIO_000772 21168233 NP860043.RA8HvaaiwH7FNrK4JVywBMSyKiBqBRTTAhwc6JgnGXU8g130_provenance.
- NP860043.RA8HvaaiwH7FNrK4JVywBMSyKiBqBRTTAhwc6JgnGXU8g130_assertion wasDerivedFrom befree-2016 NP860043.RA8HvaaiwH7FNrK4JVywBMSyKiBqBRTTAhwc6JgnGXU8g130_provenance.
- NP860043.RA8HvaaiwH7FNrK4JVywBMSyKiBqBRTTAhwc6JgnGXU8g130_assertion wasGeneratedBy ECO_0000203 NP860043.RA8HvaaiwH7FNrK4JVywBMSyKiBqBRTTAhwc6JgnGXU8g130_provenance.
- befree-2016 importedOn "2016-02-19" NP860043.RA8HvaaiwH7FNrK4JVywBMSyKiBqBRTTAhwc6JgnGXU8g130_provenance.