Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP611789.RA7TJUKGaJ_6qKKOTgCcCZPbB2SfRcDYvSGppWNniGBYk130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP611789.RA7TJUKGaJ_6qKKOTgCcCZPbB2SfRcDYvSGppWNniGBYk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP611789.RA7TJUKGaJ_6qKKOTgCcCZPbB2SfRcDYvSGppWNniGBYk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP611789.RA7TJUKGaJ_6qKKOTgCcCZPbB2SfRcDYvSGppWNniGBYk130_provenance.
- NP611789.RA7TJUKGaJ_6qKKOTgCcCZPbB2SfRcDYvSGppWNniGBYk130_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." NP611789.RA7TJUKGaJ_6qKKOTgCcCZPbB2SfRcDYvSGppWNniGBYk130_provenance.
- NP611789.RA7TJUKGaJ_6qKKOTgCcCZPbB2SfRcDYvSGppWNniGBYk130_assertion evidence source_evidence_literature NP611789.RA7TJUKGaJ_6qKKOTgCcCZPbB2SfRcDYvSGppWNniGBYk130_provenance.
- NP611789.RA7TJUKGaJ_6qKKOTgCcCZPbB2SfRcDYvSGppWNniGBYk130_assertion SIO_000772 17525745 NP611789.RA7TJUKGaJ_6qKKOTgCcCZPbB2SfRcDYvSGppWNniGBYk130_provenance.
- NP611789.RA7TJUKGaJ_6qKKOTgCcCZPbB2SfRcDYvSGppWNniGBYk130_assertion wasDerivedFrom befree-2016 NP611789.RA7TJUKGaJ_6qKKOTgCcCZPbB2SfRcDYvSGppWNniGBYk130_provenance.
- NP611789.RA7TJUKGaJ_6qKKOTgCcCZPbB2SfRcDYvSGppWNniGBYk130_assertion wasGeneratedBy ECO_0000203 NP611789.RA7TJUKGaJ_6qKKOTgCcCZPbB2SfRcDYvSGppWNniGBYk130_provenance.
- befree-2016 importedOn "2016-02-19" NP611789.RA7TJUKGaJ_6qKKOTgCcCZPbB2SfRcDYvSGppWNniGBYk130_provenance.