Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP885796.RAY4dNMskcoRZXDlJH2G8_msiOq0LlHddKgu-X4eyXq-k130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP885796.RAY4dNMskcoRZXDlJH2G8_msiOq0LlHddKgu-X4eyXq-k130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP885796.RAY4dNMskcoRZXDlJH2G8_msiOq0LlHddKgu-X4eyXq-k130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP885796.RAY4dNMskcoRZXDlJH2G8_msiOq0LlHddKgu-X4eyXq-k130_provenance.
- NP885796.RAY4dNMskcoRZXDlJH2G8_msiOq0LlHddKgu-X4eyXq-k130_assertion description "[Serotype 21 (specie B) was isolated from brain tissue and CSF of patients with acute flaccid paralysis (AFP) in Malaysia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP885796.RAY4dNMskcoRZXDlJH2G8_msiOq0LlHddKgu-X4eyXq-k130_provenance.
- NP885796.RAY4dNMskcoRZXDlJH2G8_msiOq0LlHddKgu-X4eyXq-k130_assertion evidence source_evidence_literature NP885796.RAY4dNMskcoRZXDlJH2G8_msiOq0LlHddKgu-X4eyXq-k130_provenance.
- NP885796.RAY4dNMskcoRZXDlJH2G8_msiOq0LlHddKgu-X4eyXq-k130_assertion SIO_000772 15494264 NP885796.RAY4dNMskcoRZXDlJH2G8_msiOq0LlHddKgu-X4eyXq-k130_provenance.
- NP885796.RAY4dNMskcoRZXDlJH2G8_msiOq0LlHddKgu-X4eyXq-k130_assertion wasDerivedFrom befree-20140225 NP885796.RAY4dNMskcoRZXDlJH2G8_msiOq0LlHddKgu-X4eyXq-k130_provenance.
- NP885796.RAY4dNMskcoRZXDlJH2G8_msiOq0LlHddKgu-X4eyXq-k130_assertion wasGeneratedBy ECO_0000203 NP885796.RAY4dNMskcoRZXDlJH2G8_msiOq0LlHddKgu-X4eyXq-k130_provenance.
- befree-20140225 importedOn "2014-02-25" NP885796.RAY4dNMskcoRZXDlJH2G8_msiOq0LlHddKgu-X4eyXq-k130_provenance.