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- source_evidence_literature type ECO_0000212 NP970313.RAMAnc9kk8Kz5YGaauRRyyGMJ-ayvuKqDcgh1E4EXWRMY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP970313.RAMAnc9kk8Kz5YGaauRRyyGMJ-ayvuKqDcgh1E4EXWRMY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP970313.RAMAnc9kk8Kz5YGaauRRyyGMJ-ayvuKqDcgh1E4EXWRMY130_provenance.
- NP970313.RAMAnc9kk8Kz5YGaauRRyyGMJ-ayvuKqDcgh1E4EXWRMY130_assertion description "[To determine if mutation of HGF/MET pathway genes is a mechanism for pathway dysregulation, we conducted a mutational analysis by exon resequencing of three key components of this pathway, including serine protease inhibitor Kunitz-type 1 (SPINT1), serine protease inhibitor Kunitz-type 2 (SPINT2), and MET, in 32 primary human medulloblastoma specimens.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP970313.RAMAnc9kk8Kz5YGaauRRyyGMJ-ayvuKqDcgh1E4EXWRMY130_provenance.
- NP970313.RAMAnc9kk8Kz5YGaauRRyyGMJ-ayvuKqDcgh1E4EXWRMY130_assertion evidence source_evidence_literature NP970313.RAMAnc9kk8Kz5YGaauRRyyGMJ-ayvuKqDcgh1E4EXWRMY130_provenance.
- NP970313.RAMAnc9kk8Kz5YGaauRRyyGMJ-ayvuKqDcgh1E4EXWRMY130_assertion SIO_000772 22447520 NP970313.RAMAnc9kk8Kz5YGaauRRyyGMJ-ayvuKqDcgh1E4EXWRMY130_provenance.
- NP970313.RAMAnc9kk8Kz5YGaauRRyyGMJ-ayvuKqDcgh1E4EXWRMY130_assertion wasDerivedFrom befree-2016 NP970313.RAMAnc9kk8Kz5YGaauRRyyGMJ-ayvuKqDcgh1E4EXWRMY130_provenance.
- NP970313.RAMAnc9kk8Kz5YGaauRRyyGMJ-ayvuKqDcgh1E4EXWRMY130_assertion wasGeneratedBy ECO_0000203 NP970313.RAMAnc9kk8Kz5YGaauRRyyGMJ-ayvuKqDcgh1E4EXWRMY130_provenance.
- befree-2016 importedOn "2016-02-19" NP970313.RAMAnc9kk8Kz5YGaauRRyyGMJ-ayvuKqDcgh1E4EXWRMY130_provenance.