Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP276604.RAD7Vh97pXxiTqKI9Oj3pRJwMffEzPiHVeJsq-ybFrKW8130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP276604.RAD7Vh97pXxiTqKI9Oj3pRJwMffEzPiHVeJsq-ybFrKW8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP276604.RAD7Vh97pXxiTqKI9Oj3pRJwMffEzPiHVeJsq-ybFrKW8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP276604.RAD7Vh97pXxiTqKI9Oj3pRJwMffEzPiHVeJsq-ybFrKW8130_provenance.
- NP276604.RAD7Vh97pXxiTqKI9Oj3pRJwMffEzPiHVeJsq-ybFrKW8130_assertion wasGeneratedBy ECO_0000203 NP276604.RAD7Vh97pXxiTqKI9Oj3pRJwMffEzPiHVeJsq-ybFrKW8130_provenance.
- NP276604.RAD7Vh97pXxiTqKI9Oj3pRJwMffEzPiHVeJsq-ybFrKW8130_assertion wasDerivedFrom befree-20140225 NP276604.RAD7Vh97pXxiTqKI9Oj3pRJwMffEzPiHVeJsq-ybFrKW8130_provenance.
- NP276604.RAD7Vh97pXxiTqKI9Oj3pRJwMffEzPiHVeJsq-ybFrKW8130_assertion SIO_000772 17177198 NP276604.RAD7Vh97pXxiTqKI9Oj3pRJwMffEzPiHVeJsq-ybFrKW8130_provenance.
- NP276604.RAD7Vh97pXxiTqKI9Oj3pRJwMffEzPiHVeJsq-ybFrKW8130_assertion evidence source_evidence_literature NP276604.RAD7Vh97pXxiTqKI9Oj3pRJwMffEzPiHVeJsq-ybFrKW8130_provenance.
- NP276604.RAD7Vh97pXxiTqKI9Oj3pRJwMffEzPiHVeJsq-ybFrKW8130_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." NP276604.RAD7Vh97pXxiTqKI9Oj3pRJwMffEzPiHVeJsq-ybFrKW8130_provenance.
- befree-20140225 importedOn "2014-02-25" NP276604.RAD7Vh97pXxiTqKI9Oj3pRJwMffEzPiHVeJsq-ybFrKW8130_provenance.