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- source_evidence_literature type ECO_0000212 NP785262.RA9hGuigA9zM2gKlTXqEx-wsET91qTJWu7gd2JVxaVHq4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP785262.RA9hGuigA9zM2gKlTXqEx-wsET91qTJWu7gd2JVxaVHq4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP785262.RA9hGuigA9zM2gKlTXqEx-wsET91qTJWu7gd2JVxaVHq4130_provenance.
- NP785262.RA9hGuigA9zM2gKlTXqEx-wsET91qTJWu7gd2JVxaVHq4130_assertion description "[Recently, mutations in RAF1 have been also identified in patients with NS and two patients with LEOPARD (multiple lentigines, electrocardiographic conduction abnormalities, ocular hypertelorism, pulmonary stenosis, abnormal genitalia, retardation of growth, and sensorineural deafness) syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP785262.RA9hGuigA9zM2gKlTXqEx-wsET91qTJWu7gd2JVxaVHq4130_provenance.
- NP785262.RA9hGuigA9zM2gKlTXqEx-wsET91qTJWu7gd2JVxaVHq4130_assertion evidence source_evidence_literature NP785262.RA9hGuigA9zM2gKlTXqEx-wsET91qTJWu7gd2JVxaVHq4130_provenance.
- NP785262.RA9hGuigA9zM2gKlTXqEx-wsET91qTJWu7gd2JVxaVHq4130_assertion SIO_000772 20052757 NP785262.RA9hGuigA9zM2gKlTXqEx-wsET91qTJWu7gd2JVxaVHq4130_provenance.
- NP785262.RA9hGuigA9zM2gKlTXqEx-wsET91qTJWu7gd2JVxaVHq4130_assertion wasDerivedFrom befree-2016 NP785262.RA9hGuigA9zM2gKlTXqEx-wsET91qTJWu7gd2JVxaVHq4130_provenance.
- NP785262.RA9hGuigA9zM2gKlTXqEx-wsET91qTJWu7gd2JVxaVHq4130_assertion wasGeneratedBy ECO_0000203 NP785262.RA9hGuigA9zM2gKlTXqEx-wsET91qTJWu7gd2JVxaVHq4130_provenance.
- befree-2016 importedOn "2016-02-19" NP785262.RA9hGuigA9zM2gKlTXqEx-wsET91qTJWu7gd2JVxaVHq4130_provenance.