Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP727870.RA5zRBbSdBf0amW4j2Zls1GrJGAeL-nHIe9IgnQtN0GYE130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP727870.RA5zRBbSdBf0amW4j2Zls1GrJGAeL-nHIe9IgnQtN0GYE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP727870.RA5zRBbSdBf0amW4j2Zls1GrJGAeL-nHIe9IgnQtN0GYE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP727870.RA5zRBbSdBf0amW4j2Zls1GrJGAeL-nHIe9IgnQtN0GYE130_provenance.
- NP727870.RA5zRBbSdBf0amW4j2Zls1GrJGAeL-nHIe9IgnQtN0GYE130_assertion description "[Highly penetrant, non-synonymous, or insertion-deletion mutations in TERF1 and TERF2 were not identified and therefore are not likely to be major genetic risk factors for the development of AA.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP727870.RA5zRBbSdBf0amW4j2Zls1GrJGAeL-nHIe9IgnQtN0GYE130_provenance.
- NP727870.RA5zRBbSdBf0amW4j2Zls1GrJGAeL-nHIe9IgnQtN0GYE130_assertion evidence source_evidence_literature NP727870.RA5zRBbSdBf0amW4j2Zls1GrJGAeL-nHIe9IgnQtN0GYE130_provenance.
- NP727870.RA5zRBbSdBf0amW4j2Zls1GrJGAeL-nHIe9IgnQtN0GYE130_assertion SIO_000772 16647572 NP727870.RA5zRBbSdBf0amW4j2Zls1GrJGAeL-nHIe9IgnQtN0GYE130_provenance.
- NP727870.RA5zRBbSdBf0amW4j2Zls1GrJGAeL-nHIe9IgnQtN0GYE130_assertion wasDerivedFrom befree-20150227 NP727870.RA5zRBbSdBf0amW4j2Zls1GrJGAeL-nHIe9IgnQtN0GYE130_provenance.
- NP727870.RA5zRBbSdBf0amW4j2Zls1GrJGAeL-nHIe9IgnQtN0GYE130_assertion wasGeneratedBy ECO_0000203 NP727870.RA5zRBbSdBf0amW4j2Zls1GrJGAeL-nHIe9IgnQtN0GYE130_provenance.
- befree-20150227 importedOn "2015-02-27" NP727870.RA5zRBbSdBf0amW4j2Zls1GrJGAeL-nHIe9IgnQtN0GYE130_provenance.