Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP218609.RAxcCWAmbK4wDDKFDmOPk4VeLMANHX9AdDhI4ZtanOpbg130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP218609.RAxcCWAmbK4wDDKFDmOPk4VeLMANHX9AdDhI4ZtanOpbg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP218609.RAxcCWAmbK4wDDKFDmOPk4VeLMANHX9AdDhI4ZtanOpbg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP218609.RAxcCWAmbK4wDDKFDmOPk4VeLMANHX9AdDhI4ZtanOpbg130_provenance.
- NP218609.RAxcCWAmbK4wDDKFDmOPk4VeLMANHX9AdDhI4ZtanOpbg130_assertion description "[This finding suggests that all families with a pedigree suggestive of FMTC should be regarded at risk from MEN 2A disease, at least when a critical mutation in the RET cysteine domain is detected.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP218609.RAxcCWAmbK4wDDKFDmOPk4VeLMANHX9AdDhI4ZtanOpbg130_provenance.
- NP218609.RAxcCWAmbK4wDDKFDmOPk4VeLMANHX9AdDhI4ZtanOpbg130_assertion evidence source_evidence_literature NP218609.RAxcCWAmbK4wDDKFDmOPk4VeLMANHX9AdDhI4ZtanOpbg130_provenance.
- NP218609.RAxcCWAmbK4wDDKFDmOPk4VeLMANHX9AdDhI4ZtanOpbg130_assertion SIO_000772 11280716 NP218609.RAxcCWAmbK4wDDKFDmOPk4VeLMANHX9AdDhI4ZtanOpbg130_provenance.
- NP218609.RAxcCWAmbK4wDDKFDmOPk4VeLMANHX9AdDhI4ZtanOpbg130_assertion wasDerivedFrom befree-20140225 NP218609.RAxcCWAmbK4wDDKFDmOPk4VeLMANHX9AdDhI4ZtanOpbg130_provenance.
- NP218609.RAxcCWAmbK4wDDKFDmOPk4VeLMANHX9AdDhI4ZtanOpbg130_assertion wasGeneratedBy ECO_0000203 NP218609.RAxcCWAmbK4wDDKFDmOPk4VeLMANHX9AdDhI4ZtanOpbg130_provenance.
- befree-20140225 importedOn "2014-02-25" NP218609.RAxcCWAmbK4wDDKFDmOPk4VeLMANHX9AdDhI4ZtanOpbg130_provenance.