Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP401641.RA-mRxX9fNZDBB7IiVm-6bXVqoKndPue3qaF4SCx_xY-M130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP401641.RA-mRxX9fNZDBB7IiVm-6bXVqoKndPue3qaF4SCx_xY-M130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP401641.RA-mRxX9fNZDBB7IiVm-6bXVqoKndPue3qaF4SCx_xY-M130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP401641.RA-mRxX9fNZDBB7IiVm-6bXVqoKndPue3qaF4SCx_xY-M130_provenance.
- NP401641.RA-mRxX9fNZDBB7IiVm-6bXVqoKndPue3qaF4SCx_xY-M130_assertion description "[Q289P mutation in the FGFR2 gene: first report in a patient with type 1 Pfeiffer syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP401641.RA-mRxX9fNZDBB7IiVm-6bXVqoKndPue3qaF4SCx_xY-M130_provenance.
- NP401641.RA-mRxX9fNZDBB7IiVm-6bXVqoKndPue3qaF4SCx_xY-M130_assertion evidence source_evidence_literature NP401641.RA-mRxX9fNZDBB7IiVm-6bXVqoKndPue3qaF4SCx_xY-M130_provenance.
- NP401641.RA-mRxX9fNZDBB7IiVm-6bXVqoKndPue3qaF4SCx_xY-M130_assertion SIO_000772 19066959 NP401641.RA-mRxX9fNZDBB7IiVm-6bXVqoKndPue3qaF4SCx_xY-M130_provenance.
- NP401641.RA-mRxX9fNZDBB7IiVm-6bXVqoKndPue3qaF4SCx_xY-M130_assertion wasDerivedFrom befree-20150227 NP401641.RA-mRxX9fNZDBB7IiVm-6bXVqoKndPue3qaF4SCx_xY-M130_provenance.
- NP401641.RA-mRxX9fNZDBB7IiVm-6bXVqoKndPue3qaF4SCx_xY-M130_assertion wasGeneratedBy ECO_0000203 NP401641.RA-mRxX9fNZDBB7IiVm-6bXVqoKndPue3qaF4SCx_xY-M130_provenance.
- befree-20150227 importedOn "2015-02-27" NP401641.RA-mRxX9fNZDBB7IiVm-6bXVqoKndPue3qaF4SCx_xY-M130_provenance.