Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP908594.RAZ7NnBL6hx18lp5TKDGEPPCa5h4UCRighQg4Yrm_1Vmc130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP908594.RAZ7NnBL6hx18lp5TKDGEPPCa5h4UCRighQg4Yrm_1Vmc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP908594.RAZ7NnBL6hx18lp5TKDGEPPCa5h4UCRighQg4Yrm_1Vmc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP908594.RAZ7NnBL6hx18lp5TKDGEPPCa5h4UCRighQg4Yrm_1Vmc130_provenance.
- NP908594.RAZ7NnBL6hx18lp5TKDGEPPCa5h4UCRighQg4Yrm_1Vmc130_assertion description "[Mutation analysis of the SHOC2 gene in Noonan-like syndrome and in hematologic malignancies.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP908594.RAZ7NnBL6hx18lp5TKDGEPPCa5h4UCRighQg4Yrm_1Vmc130_provenance.
- NP908594.RAZ7NnBL6hx18lp5TKDGEPPCa5h4UCRighQg4Yrm_1Vmc130_assertion evidence source_evidence_literature NP908594.RAZ7NnBL6hx18lp5TKDGEPPCa5h4UCRighQg4Yrm_1Vmc130_provenance.
- NP908594.RAZ7NnBL6hx18lp5TKDGEPPCa5h4UCRighQg4Yrm_1Vmc130_assertion SIO_000772 20882035 NP908594.RAZ7NnBL6hx18lp5TKDGEPPCa5h4UCRighQg4Yrm_1Vmc130_provenance.
- NP908594.RAZ7NnBL6hx18lp5TKDGEPPCa5h4UCRighQg4Yrm_1Vmc130_assertion wasDerivedFrom befree-20140225 NP908594.RAZ7NnBL6hx18lp5TKDGEPPCa5h4UCRighQg4Yrm_1Vmc130_provenance.
- NP908594.RAZ7NnBL6hx18lp5TKDGEPPCa5h4UCRighQg4Yrm_1Vmc130_assertion wasGeneratedBy ECO_0000203 NP908594.RAZ7NnBL6hx18lp5TKDGEPPCa5h4UCRighQg4Yrm_1Vmc130_provenance.
- befree-20140225 importedOn "2014-02-25" NP908594.RAZ7NnBL6hx18lp5TKDGEPPCa5h4UCRighQg4Yrm_1Vmc130_provenance.