Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP298861.RA_b1rMMhtLaMlvNVk5q_MmdLzibP9W5bHe4Lc1CEy6mc130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP298861.RA_b1rMMhtLaMlvNVk5q_MmdLzibP9W5bHe4Lc1CEy6mc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP298861.RA_b1rMMhtLaMlvNVk5q_MmdLzibP9W5bHe4Lc1CEy6mc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP298861.RA_b1rMMhtLaMlvNVk5q_MmdLzibP9W5bHe4Lc1CEy6mc130_provenance.
- NP298861.RA_b1rMMhtLaMlvNVk5q_MmdLzibP9W5bHe4Lc1CEy6mc130_assertion description "[Two missense mutations in this codon are known to result in strong constitutive activation of the FGFR3 tyrosine kinase and cause three different skeletal dysplasia syndromes-thanatophoric dysplasia type II (TD2) (A1948G [Lys650Glu]) and SADDAN (severe achondroplasia with developmental delay and acanthosis nigricans) syndrome and thanatophoric dysplasia type I (TD1) (both due to A1949T [Lys650Met]).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP298861.RA_b1rMMhtLaMlvNVk5q_MmdLzibP9W5bHe4Lc1CEy6mc130_provenance.
- NP298861.RA_b1rMMhtLaMlvNVk5q_MmdLzibP9W5bHe4Lc1CEy6mc130_assertion evidence source_evidence_literature NP298861.RA_b1rMMhtLaMlvNVk5q_MmdLzibP9W5bHe4Lc1CEy6mc130_provenance.
- NP298861.RA_b1rMMhtLaMlvNVk5q_MmdLzibP9W5bHe4Lc1CEy6mc130_assertion SIO_000772 11055896 NP298861.RA_b1rMMhtLaMlvNVk5q_MmdLzibP9W5bHe4Lc1CEy6mc130_provenance.
- NP298861.RA_b1rMMhtLaMlvNVk5q_MmdLzibP9W5bHe4Lc1CEy6mc130_assertion wasDerivedFrom befree-2016 NP298861.RA_b1rMMhtLaMlvNVk5q_MmdLzibP9W5bHe4Lc1CEy6mc130_provenance.
- NP298861.RA_b1rMMhtLaMlvNVk5q_MmdLzibP9W5bHe4Lc1CEy6mc130_assertion wasGeneratedBy ECO_0000203 NP298861.RA_b1rMMhtLaMlvNVk5q_MmdLzibP9W5bHe4Lc1CEy6mc130_provenance.
- befree-2016 importedOn "2016-02-19" NP298861.RA_b1rMMhtLaMlvNVk5q_MmdLzibP9W5bHe4Lc1CEy6mc130_provenance.