Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP660660.RAHJsUUXG7RU68ZjiKpyFw4c4hRgAeY46b2ETsa6yFZA0130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP660660.RAHJsUUXG7RU68ZjiKpyFw4c4hRgAeY46b2ETsa6yFZA0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP660660.RAHJsUUXG7RU68ZjiKpyFw4c4hRgAeY46b2ETsa6yFZA0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP660660.RAHJsUUXG7RU68ZjiKpyFw4c4hRgAeY46b2ETsa6yFZA0130_provenance.
- befree-20150227 importedOn "2015-02-27" NP660660.RAHJsUUXG7RU68ZjiKpyFw4c4hRgAeY46b2ETsa6yFZA0130_provenance.
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- NP660660.RAHJsUUXG7RU68ZjiKpyFw4c4hRgAeY46b2ETsa6yFZA0130_assertion wasDerivedFrom befree-20150227 NP660660.RAHJsUUXG7RU68ZjiKpyFw4c4hRgAeY46b2ETsa6yFZA0130_provenance.
- NP660660.RAHJsUUXG7RU68ZjiKpyFw4c4hRgAeY46b2ETsa6yFZA0130_assertion SIO_000772 17177198 NP660660.RAHJsUUXG7RU68ZjiKpyFw4c4hRgAeY46b2ETsa6yFZA0130_provenance.
- NP660660.RAHJsUUXG7RU68ZjiKpyFw4c4hRgAeY46b2ETsa6yFZA0130_assertion evidence source_evidence_literature NP660660.RAHJsUUXG7RU68ZjiKpyFw4c4hRgAeY46b2ETsa6yFZA0130_provenance.
- NP660660.RAHJsUUXG7RU68ZjiKpyFw4c4hRgAeY46b2ETsa6yFZA0130_assertion description "[Mutations of the protein tyrosine phosphatase SHP-2 are implicated in human diseases, causing Noonan syndrome (NS) and related developmental disorders or contributing to leukemogenesis depending on the specific amino acid substitution involved.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP660660.RAHJsUUXG7RU68ZjiKpyFw4c4hRgAeY46b2ETsa6yFZA0130_provenance.