Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP767594.RADKZvGPs756xhCY2F7Aoak5-0fR3uAmZPTdQWnBSNp_0130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP767594.RADKZvGPs756xhCY2F7Aoak5-0fR3uAmZPTdQWnBSNp_0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP767594.RADKZvGPs756xhCY2F7Aoak5-0fR3uAmZPTdQWnBSNp_0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP767594.RADKZvGPs756xhCY2F7Aoak5-0fR3uAmZPTdQWnBSNp_0130_provenance.
- befree-20150227 importedOn "2015-02-27" NP767594.RADKZvGPs756xhCY2F7Aoak5-0fR3uAmZPTdQWnBSNp_0130_provenance.
- NP767594.RADKZvGPs756xhCY2F7Aoak5-0fR3uAmZPTdQWnBSNp_0130_assertion wasGeneratedBy ECO_0000203 NP767594.RADKZvGPs756xhCY2F7Aoak5-0fR3uAmZPTdQWnBSNp_0130_provenance.
- NP767594.RADKZvGPs756xhCY2F7Aoak5-0fR3uAmZPTdQWnBSNp_0130_assertion wasDerivedFrom befree-20150227 NP767594.RADKZvGPs756xhCY2F7Aoak5-0fR3uAmZPTdQWnBSNp_0130_provenance.
- NP767594.RADKZvGPs756xhCY2F7Aoak5-0fR3uAmZPTdQWnBSNp_0130_assertion SIO_000772 22004887 NP767594.RADKZvGPs756xhCY2F7Aoak5-0fR3uAmZPTdQWnBSNp_0130_provenance.
- NP767594.RADKZvGPs756xhCY2F7Aoak5-0fR3uAmZPTdQWnBSNp_0130_assertion evidence source_evidence_literature NP767594.RADKZvGPs756xhCY2F7Aoak5-0fR3uAmZPTdQWnBSNp_0130_provenance.
- NP767594.RADKZvGPs756xhCY2F7Aoak5-0fR3uAmZPTdQWnBSNp_0130_assertion description "[This report provide a wide spectrum of USH2A mutations and clinical features, including atypical Usher syndrome phenotypes resembling Usher syndrome type I.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP767594.RADKZvGPs756xhCY2F7Aoak5-0fR3uAmZPTdQWnBSNp_0130_provenance.