Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP324429.RAxLBWm1jv6u0341QxBSFxTOwb6LMcibO2FjN0kYTVqn4130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP324429.RAxLBWm1jv6u0341QxBSFxTOwb6LMcibO2FjN0kYTVqn4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP324429.RAxLBWm1jv6u0341QxBSFxTOwb6LMcibO2FjN0kYTVqn4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP324429.RAxLBWm1jv6u0341QxBSFxTOwb6LMcibO2FjN0kYTVqn4130_provenance.
- NP324429.RAxLBWm1jv6u0341QxBSFxTOwb6LMcibO2FjN0kYTVqn4130_assertion description "[The combined data show that p63 is the major gene for EEC syndrome, and that it makes a modest contribution to SHFM.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP324429.RAxLBWm1jv6u0341QxBSFxTOwb6LMcibO2FjN0kYTVqn4130_provenance.
- NP324429.RAxLBWm1jv6u0341QxBSFxTOwb6LMcibO2FjN0kYTVqn4130_assertion evidence source_evidence_literature NP324429.RAxLBWm1jv6u0341QxBSFxTOwb6LMcibO2FjN0kYTVqn4130_provenance.
- NP324429.RAxLBWm1jv6u0341QxBSFxTOwb6LMcibO2FjN0kYTVqn4130_assertion SIO_000772 11462173 NP324429.RAxLBWm1jv6u0341QxBSFxTOwb6LMcibO2FjN0kYTVqn4130_provenance.
- NP324429.RAxLBWm1jv6u0341QxBSFxTOwb6LMcibO2FjN0kYTVqn4130_assertion wasDerivedFrom befree-2016 NP324429.RAxLBWm1jv6u0341QxBSFxTOwb6LMcibO2FjN0kYTVqn4130_provenance.
- NP324429.RAxLBWm1jv6u0341QxBSFxTOwb6LMcibO2FjN0kYTVqn4130_assertion wasGeneratedBy ECO_0000203 NP324429.RAxLBWm1jv6u0341QxBSFxTOwb6LMcibO2FjN0kYTVqn4130_provenance.
- befree-2016 importedOn "2016-02-19" NP324429.RAxLBWm1jv6u0341QxBSFxTOwb6LMcibO2FjN0kYTVqn4130_provenance.