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- source_evidence_literature type ECO_0000212 NP394873.RAyj9kFcVQJUO0-T_Io4nE9zI0--zNj1LXsymTlgZW4lI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP394873.RAyj9kFcVQJUO0-T_Io4nE9zI0--zNj1LXsymTlgZW4lI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP394873.RAyj9kFcVQJUO0-T_Io4nE9zI0--zNj1LXsymTlgZW4lI130_provenance.
- NP394873.RAyj9kFcVQJUO0-T_Io4nE9zI0--zNj1LXsymTlgZW4lI130_assertion description "[The fibulin-1 gene (FBLN1) is disrupted in a t(12;22) associated with a complex type of synpolydactyly.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP394873.RAyj9kFcVQJUO0-T_Io4nE9zI0--zNj1LXsymTlgZW4lI130_provenance.
- NP394873.RAyj9kFcVQJUO0-T_Io4nE9zI0--zNj1LXsymTlgZW4lI130_assertion evidence source_evidence_literature NP394873.RAyj9kFcVQJUO0-T_Io4nE9zI0--zNj1LXsymTlgZW4lI130_provenance.
- NP394873.RAyj9kFcVQJUO0-T_Io4nE9zI0--zNj1LXsymTlgZW4lI130_assertion SIO_000772 11836357 NP394873.RAyj9kFcVQJUO0-T_Io4nE9zI0--zNj1LXsymTlgZW4lI130_provenance.
- NP394873.RAyj9kFcVQJUO0-T_Io4nE9zI0--zNj1LXsymTlgZW4lI130_assertion wasDerivedFrom befree-20150227 NP394873.RAyj9kFcVQJUO0-T_Io4nE9zI0--zNj1LXsymTlgZW4lI130_provenance.
- NP394873.RAyj9kFcVQJUO0-T_Io4nE9zI0--zNj1LXsymTlgZW4lI130_assertion wasGeneratedBy ECO_0000203 NP394873.RAyj9kFcVQJUO0-T_Io4nE9zI0--zNj1LXsymTlgZW4lI130_provenance.
- befree-20150227 importedOn "2015-02-27" NP394873.RAyj9kFcVQJUO0-T_Io4nE9zI0--zNj1LXsymTlgZW4lI130_provenance.