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- source_evidence_literature type ECO_0000212 NP877839.RATkWYbAcBvIuiD2Lkoij-2wXxkz8ZTl5P3RV0_7sSJ3Y130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP877839.RATkWYbAcBvIuiD2Lkoij-2wXxkz8ZTl5P3RV0_7sSJ3Y130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP877839.RATkWYbAcBvIuiD2Lkoij-2wXxkz8ZTl5P3RV0_7sSJ3Y130_provenance.
- NP877839.RATkWYbAcBvIuiD2Lkoij-2wXxkz8ZTl5P3RV0_7sSJ3Y130_assertion description "[In the present study an FSCN2 mutation was examined that has been reported, not only in patients with retinitis pigmentosa (RP), but also in the normal population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP877839.RATkWYbAcBvIuiD2Lkoij-2wXxkz8ZTl5P3RV0_7sSJ3Y130_provenance.
- NP877839.RATkWYbAcBvIuiD2Lkoij-2wXxkz8ZTl5P3RV0_7sSJ3Y130_assertion evidence source_evidence_literature NP877839.RATkWYbAcBvIuiD2Lkoij-2wXxkz8ZTl5P3RV0_7sSJ3Y130_provenance.
- NP877839.RATkWYbAcBvIuiD2Lkoij-2wXxkz8ZTl5P3RV0_7sSJ3Y130_assertion SIO_000772 18450588 NP877839.RATkWYbAcBvIuiD2Lkoij-2wXxkz8ZTl5P3RV0_7sSJ3Y130_provenance.
- NP877839.RATkWYbAcBvIuiD2Lkoij-2wXxkz8ZTl5P3RV0_7sSJ3Y130_assertion wasDerivedFrom befree-20150227 NP877839.RATkWYbAcBvIuiD2Lkoij-2wXxkz8ZTl5P3RV0_7sSJ3Y130_provenance.
- NP877839.RATkWYbAcBvIuiD2Lkoij-2wXxkz8ZTl5P3RV0_7sSJ3Y130_assertion wasGeneratedBy ECO_0000203 NP877839.RATkWYbAcBvIuiD2Lkoij-2wXxkz8ZTl5P3RV0_7sSJ3Y130_provenance.
- befree-20150227 importedOn "2015-02-27" NP877839.RATkWYbAcBvIuiD2Lkoij-2wXxkz8ZTl5P3RV0_7sSJ3Y130_provenance.