Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP858882.RAtCPfwyyhlaxO38fUoAOMtcoa2fE4Pldw2ghedj8w3tc130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP858882.RAtCPfwyyhlaxO38fUoAOMtcoa2fE4Pldw2ghedj8w3tc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP858882.RAtCPfwyyhlaxO38fUoAOMtcoa2fE4Pldw2ghedj8w3tc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP858882.RAtCPfwyyhlaxO38fUoAOMtcoa2fE4Pldw2ghedj8w3tc130_provenance.
- NP858882.RAtCPfwyyhlaxO38fUoAOMtcoa2fE4Pldw2ghedj8w3tc130_assertion description "[Given that there are other eight MRX families overlapping this interval, none of them with known mutation, we conclude that at least one new gene responsible for nonsyndromic mental retardation is located in this region.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP858882.RAtCPfwyyhlaxO38fUoAOMtcoa2fE4Pldw2ghedj8w3tc130_provenance.
- NP858882.RAtCPfwyyhlaxO38fUoAOMtcoa2fE4Pldw2ghedj8w3tc130_assertion evidence source_evidence_literature NP858882.RAtCPfwyyhlaxO38fUoAOMtcoa2fE4Pldw2ghedj8w3tc130_provenance.
- NP858882.RAtCPfwyyhlaxO38fUoAOMtcoa2fE4Pldw2ghedj8w3tc130_assertion SIO_000772 15526294 NP858882.RAtCPfwyyhlaxO38fUoAOMtcoa2fE4Pldw2ghedj8w3tc130_provenance.
- NP858882.RAtCPfwyyhlaxO38fUoAOMtcoa2fE4Pldw2ghedj8w3tc130_assertion wasDerivedFrom befree-20140225 NP858882.RAtCPfwyyhlaxO38fUoAOMtcoa2fE4Pldw2ghedj8w3tc130_provenance.
- NP858882.RAtCPfwyyhlaxO38fUoAOMtcoa2fE4Pldw2ghedj8w3tc130_assertion wasGeneratedBy ECO_0000203 NP858882.RAtCPfwyyhlaxO38fUoAOMtcoa2fE4Pldw2ghedj8w3tc130_provenance.
- befree-20140225 importedOn "2014-02-25" NP858882.RAtCPfwyyhlaxO38fUoAOMtcoa2fE4Pldw2ghedj8w3tc130_provenance.