Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP935451.RA1Tn5UUU2t5qIAhG0SQEENN79hkLmiglBkWkVPid-GJM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP935451.RA1Tn5UUU2t5qIAhG0SQEENN79hkLmiglBkWkVPid-GJM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP935451.RA1Tn5UUU2t5qIAhG0SQEENN79hkLmiglBkWkVPid-GJM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP935451.RA1Tn5UUU2t5qIAhG0SQEENN79hkLmiglBkWkVPid-GJM130_provenance.
- NP935451.RA1Tn5UUU2t5qIAhG0SQEENN79hkLmiglBkWkVPid-GJM130_assertion description "[In 1994, the field of bone biology was significantly advanced by the discovery that activating mutations in the fibroblast growth factor receptor 3 (FGFR3) receptor tyrosine kinase (TK) account for the common genetic form of dwarfism in humans, achondroplasia (ACH).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP935451.RA1Tn5UUU2t5qIAhG0SQEENN79hkLmiglBkWkVPid-GJM130_provenance.
- NP935451.RA1Tn5UUU2t5qIAhG0SQEENN79hkLmiglBkWkVPid-GJM130_assertion evidence source_evidence_literature NP935451.RA1Tn5UUU2t5qIAhG0SQEENN79hkLmiglBkWkVPid-GJM130_provenance.
- NP935451.RA1Tn5UUU2t5qIAhG0SQEENN79hkLmiglBkWkVPid-GJM130_assertion SIO_000772 22045636 NP935451.RA1Tn5UUU2t5qIAhG0SQEENN79hkLmiglBkWkVPid-GJM130_provenance.
- NP935451.RA1Tn5UUU2t5qIAhG0SQEENN79hkLmiglBkWkVPid-GJM130_assertion wasDerivedFrom befree-2016 NP935451.RA1Tn5UUU2t5qIAhG0SQEENN79hkLmiglBkWkVPid-GJM130_provenance.
- NP935451.RA1Tn5UUU2t5qIAhG0SQEENN79hkLmiglBkWkVPid-GJM130_assertion wasGeneratedBy ECO_0000203 NP935451.RA1Tn5UUU2t5qIAhG0SQEENN79hkLmiglBkWkVPid-GJM130_provenance.
- befree-2016 importedOn "2016-02-19" NP935451.RA1Tn5UUU2t5qIAhG0SQEENN79hkLmiglBkWkVPid-GJM130_provenance.