Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP852581.RAA6WHpESNU_-pinzforxyX1sr3-WR-maiicMiEQbvvuk130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP852581.RAA6WHpESNU_-pinzforxyX1sr3-WR-maiicMiEQbvvuk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP852581.RAA6WHpESNU_-pinzforxyX1sr3-WR-maiicMiEQbvvuk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP852581.RAA6WHpESNU_-pinzforxyX1sr3-WR-maiicMiEQbvvuk130_provenance.
- NP852581.RAA6WHpESNU_-pinzforxyX1sr3-WR-maiicMiEQbvvuk130_assertion description "[All the other loci analyzed were altered in less than 40% of cases and some of them (D3S1312, D3S1300, IFNA, D9S164, D13S176 and TP53) did not show alterations in any of the ameloblastomas analyzed.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP852581.RAA6WHpESNU_-pinzforxyX1sr3-WR-maiicMiEQbvvuk130_provenance.
- NP852581.RAA6WHpESNU_-pinzforxyX1sr3-WR-maiicMiEQbvvuk130_assertion evidence source_evidence_literature NP852581.RAA6WHpESNU_-pinzforxyX1sr3-WR-maiicMiEQbvvuk130_provenance.
- NP852581.RAA6WHpESNU_-pinzforxyX1sr3-WR-maiicMiEQbvvuk130_assertion SIO_000772 17307020 NP852581.RAA6WHpESNU_-pinzforxyX1sr3-WR-maiicMiEQbvvuk130_provenance.
- NP852581.RAA6WHpESNU_-pinzforxyX1sr3-WR-maiicMiEQbvvuk130_assertion wasDerivedFrom befree-20140225 NP852581.RAA6WHpESNU_-pinzforxyX1sr3-WR-maiicMiEQbvvuk130_provenance.
- NP852581.RAA6WHpESNU_-pinzforxyX1sr3-WR-maiicMiEQbvvuk130_assertion wasGeneratedBy ECO_0000203 NP852581.RAA6WHpESNU_-pinzforxyX1sr3-WR-maiicMiEQbvvuk130_provenance.
- befree-20140225 importedOn "2014-02-25" NP852581.RAA6WHpESNU_-pinzforxyX1sr3-WR-maiicMiEQbvvuk130_provenance.