Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP107366.RAPP5y3WLch4DSQnQ3XZ72r2kU1J69jA6SkQPhEmNRK9Q130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP107366.RAPP5y3WLch4DSQnQ3XZ72r2kU1J69jA6SkQPhEmNRK9Q130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP107366.RAPP5y3WLch4DSQnQ3XZ72r2kU1J69jA6SkQPhEmNRK9Q130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP107366.RAPP5y3WLch4DSQnQ3XZ72r2kU1J69jA6SkQPhEmNRK9Q130_provenance.
- NP107366.RAPP5y3WLch4DSQnQ3XZ72r2kU1J69jA6SkQPhEmNRK9Q130_assertion description "[Patients with childhood ALCL have a higher probability of being a carrier of a PRF1 mutation compared with healthy controls, suggesting a possible predisposing role.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP107366.RAPP5y3WLch4DSQnQ3XZ72r2kU1J69jA6SkQPhEmNRK9Q130_provenance.
- NP107366.RAPP5y3WLch4DSQnQ3XZ72r2kU1J69jA6SkQPhEmNRK9Q130_assertion evidence source_evidence_literature NP107366.RAPP5y3WLch4DSQnQ3XZ72r2kU1J69jA6SkQPhEmNRK9Q130_provenance.
- NP107366.RAPP5y3WLch4DSQnQ3XZ72r2kU1J69jA6SkQPhEmNRK9Q130_assertion SIO_000772 17477373 NP107366.RAPP5y3WLch4DSQnQ3XZ72r2kU1J69jA6SkQPhEmNRK9Q130_provenance.
- NP107366.RAPP5y3WLch4DSQnQ3XZ72r2kU1J69jA6SkQPhEmNRK9Q130_assertion wasDerivedFrom gad-20150221 NP107366.RAPP5y3WLch4DSQnQ3XZ72r2kU1J69jA6SkQPhEmNRK9Q130_provenance.
- NP107366.RAPP5y3WLch4DSQnQ3XZ72r2kU1J69jA6SkQPhEmNRK9Q130_assertion wasGeneratedBy ECO_0000203 NP107366.RAPP5y3WLch4DSQnQ3XZ72r2kU1J69jA6SkQPhEmNRK9Q130_provenance.
- gad-20150221 importedOn "2015-02-21" NP107366.RAPP5y3WLch4DSQnQ3XZ72r2kU1J69jA6SkQPhEmNRK9Q130_provenance.