Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1245088.RAehc2aJ9GNOmvEYLjcCdpYTkyc_0KdA2jnQ1T9yuX-C8130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1245088.RAehc2aJ9GNOmvEYLjcCdpYTkyc_0KdA2jnQ1T9yuX-C8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1245088.RAehc2aJ9GNOmvEYLjcCdpYTkyc_0KdA2jnQ1T9yuX-C8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1245088.RAehc2aJ9GNOmvEYLjcCdpYTkyc_0KdA2jnQ1T9yuX-C8130_provenance.
- NP1245088.RAehc2aJ9GNOmvEYLjcCdpYTkyc_0KdA2jnQ1T9yuX-C8130_assertion description "[Functional testing strategy for coding genetic variants of unclear significance in MLH1 in Lynch syndrome diagnosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1245088.RAehc2aJ9GNOmvEYLjcCdpYTkyc_0KdA2jnQ1T9yuX-C8130_provenance.
- NP1245088.RAehc2aJ9GNOmvEYLjcCdpYTkyc_0KdA2jnQ1T9yuX-C8130_assertion evidence source_evidence_literature NP1245088.RAehc2aJ9GNOmvEYLjcCdpYTkyc_0KdA2jnQ1T9yuX-C8130_provenance.
- NP1245088.RAehc2aJ9GNOmvEYLjcCdpYTkyc_0KdA2jnQ1T9yuX-C8130_assertion SIO_000772 25477341 NP1245088.RAehc2aJ9GNOmvEYLjcCdpYTkyc_0KdA2jnQ1T9yuX-C8130_provenance.
- NP1245088.RAehc2aJ9GNOmvEYLjcCdpYTkyc_0KdA2jnQ1T9yuX-C8130_assertion wasDerivedFrom befree-2016 NP1245088.RAehc2aJ9GNOmvEYLjcCdpYTkyc_0KdA2jnQ1T9yuX-C8130_provenance.
- NP1245088.RAehc2aJ9GNOmvEYLjcCdpYTkyc_0KdA2jnQ1T9yuX-C8130_assertion wasGeneratedBy ECO_0000203 NP1245088.RAehc2aJ9GNOmvEYLjcCdpYTkyc_0KdA2jnQ1T9yuX-C8130_provenance.
- befree-2016 importedOn "2016-02-19" NP1245088.RAehc2aJ9GNOmvEYLjcCdpYTkyc_0KdA2jnQ1T9yuX-C8130_provenance.