Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP640176.RAxqu9FJ0QioE-8pAVBeJVINpNjq0V9PhNB6w-ILQU1fk130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP640176.RAxqu9FJ0QioE-8pAVBeJVINpNjq0V9PhNB6w-ILQU1fk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP640176.RAxqu9FJ0QioE-8pAVBeJVINpNjq0V9PhNB6w-ILQU1fk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP640176.RAxqu9FJ0QioE-8pAVBeJVINpNjq0V9PhNB6w-ILQU1fk130_provenance.
- NP640176.RAxqu9FJ0QioE-8pAVBeJVINpNjq0V9PhNB6w-ILQU1fk130_assertion description "[Thus, our findings implicate RAF1 gain-of-function mutations as a causative agent of a human developmental disorder, representing a new genetic mechanism for the activation of the MAPK pathway.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP640176.RAxqu9FJ0QioE-8pAVBeJVINpNjq0V9PhNB6w-ILQU1fk130_provenance.
- NP640176.RAxqu9FJ0QioE-8pAVBeJVINpNjq0V9PhNB6w-ILQU1fk130_assertion evidence source_evidence_literature NP640176.RAxqu9FJ0QioE-8pAVBeJVINpNjq0V9PhNB6w-ILQU1fk130_provenance.
- NP640176.RAxqu9FJ0QioE-8pAVBeJVINpNjq0V9PhNB6w-ILQU1fk130_assertion SIO_000772 17603482 NP640176.RAxqu9FJ0QioE-8pAVBeJVINpNjq0V9PhNB6w-ILQU1fk130_provenance.
- NP640176.RAxqu9FJ0QioE-8pAVBeJVINpNjq0V9PhNB6w-ILQU1fk130_assertion wasDerivedFrom befree-20140225 NP640176.RAxqu9FJ0QioE-8pAVBeJVINpNjq0V9PhNB6w-ILQU1fk130_provenance.
- NP640176.RAxqu9FJ0QioE-8pAVBeJVINpNjq0V9PhNB6w-ILQU1fk130_assertion wasGeneratedBy ECO_0000203 NP640176.RAxqu9FJ0QioE-8pAVBeJVINpNjq0V9PhNB6w-ILQU1fk130_provenance.
- befree-20140225 importedOn "2014-02-25" NP640176.RAxqu9FJ0QioE-8pAVBeJVINpNjq0V9PhNB6w-ILQU1fk130_provenance.