Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP400794.RA0j0k-GdJWuDTlWydHMsbKMtiy2xW9TvrGeUFSS-F-Bo130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP400794.RA0j0k-GdJWuDTlWydHMsbKMtiy2xW9TvrGeUFSS-F-Bo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP400794.RA0j0k-GdJWuDTlWydHMsbKMtiy2xW9TvrGeUFSS-F-Bo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP400794.RA0j0k-GdJWuDTlWydHMsbKMtiy2xW9TvrGeUFSS-F-Bo130_provenance.
- NP400794.RA0j0k-GdJWuDTlWydHMsbKMtiy2xW9TvrGeUFSS-F-Bo130_assertion description "[The majority of the somatic mutations identified were identical to germline activating mutations in FGFR2 and FGFR3 that cause Apert Syndrome, Beare-Stevenson Syndrome, hypochondroplasia, achondroplasia and SADDAN syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP400794.RA0j0k-GdJWuDTlWydHMsbKMtiy2xW9TvrGeUFSS-F-Bo130_provenance.
- NP400794.RA0j0k-GdJWuDTlWydHMsbKMtiy2xW9TvrGeUFSS-F-Bo130_assertion evidence source_evidence_literature NP400794.RA0j0k-GdJWuDTlWydHMsbKMtiy2xW9TvrGeUFSS-F-Bo130_provenance.
- NP400794.RA0j0k-GdJWuDTlWydHMsbKMtiy2xW9TvrGeUFSS-F-Bo130_assertion SIO_000772 17525745 NP400794.RA0j0k-GdJWuDTlWydHMsbKMtiy2xW9TvrGeUFSS-F-Bo130_provenance.
- NP400794.RA0j0k-GdJWuDTlWydHMsbKMtiy2xW9TvrGeUFSS-F-Bo130_assertion wasDerivedFrom befree-20150227 NP400794.RA0j0k-GdJWuDTlWydHMsbKMtiy2xW9TvrGeUFSS-F-Bo130_provenance.
- NP400794.RA0j0k-GdJWuDTlWydHMsbKMtiy2xW9TvrGeUFSS-F-Bo130_assertion wasGeneratedBy ECO_0000203 NP400794.RA0j0k-GdJWuDTlWydHMsbKMtiy2xW9TvrGeUFSS-F-Bo130_provenance.
- befree-20150227 importedOn "2015-02-27" NP400794.RA0j0k-GdJWuDTlWydHMsbKMtiy2xW9TvrGeUFSS-F-Bo130_provenance.