Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP842733.RA3-UMjTx62Zr0UR3FGHrrDtH3p1fgiteoT_Kog8zX1tY130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP842733.RA3-UMjTx62Zr0UR3FGHrrDtH3p1fgiteoT_Kog8zX1tY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP842733.RA3-UMjTx62Zr0UR3FGHrrDtH3p1fgiteoT_Kog8zX1tY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP842733.RA3-UMjTx62Zr0UR3FGHrrDtH3p1fgiteoT_Kog8zX1tY130_provenance.
- NP842733.RA3-UMjTx62Zr0UR3FGHrrDtH3p1fgiteoT_Kog8zX1tY130_assertion description "[In order to understand the contribution of SHOC2 mutations to the clinical manifestations of Noonan syndrome and related disorders, we analyzed SHOC2 in 92 patients with Noonan syndrome and related disorders who did not exhibit PTPN11, KRAS, HRAS, BRAF, MAP2K1/2, SOS1 or RAF1 mutations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP842733.RA3-UMjTx62Zr0UR3FGHrrDtH3p1fgiteoT_Kog8zX1tY130_provenance.
- NP842733.RA3-UMjTx62Zr0UR3FGHrrDtH3p1fgiteoT_Kog8zX1tY130_assertion evidence source_evidence_literature NP842733.RA3-UMjTx62Zr0UR3FGHrrDtH3p1fgiteoT_Kog8zX1tY130_provenance.
- NP842733.RA3-UMjTx62Zr0UR3FGHrrDtH3p1fgiteoT_Kog8zX1tY130_assertion SIO_000772 20882035 NP842733.RA3-UMjTx62Zr0UR3FGHrrDtH3p1fgiteoT_Kog8zX1tY130_provenance.
- NP842733.RA3-UMjTx62Zr0UR3FGHrrDtH3p1fgiteoT_Kog8zX1tY130_assertion wasDerivedFrom befree-2016 NP842733.RA3-UMjTx62Zr0UR3FGHrrDtH3p1fgiteoT_Kog8zX1tY130_provenance.
- NP842733.RA3-UMjTx62Zr0UR3FGHrrDtH3p1fgiteoT_Kog8zX1tY130_assertion wasGeneratedBy ECO_0000203 NP842733.RA3-UMjTx62Zr0UR3FGHrrDtH3p1fgiteoT_Kog8zX1tY130_provenance.
- befree-2016 importedOn "2016-02-19" NP842733.RA3-UMjTx62Zr0UR3FGHrrDtH3p1fgiteoT_Kog8zX1tY130_provenance.