Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP395891.RA4YRDmvPBZ9JU2XY2LmskdffkOrritBZfGyl3r7nVBRY130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP395891.RA4YRDmvPBZ9JU2XY2LmskdffkOrritBZfGyl3r7nVBRY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP395891.RA4YRDmvPBZ9JU2XY2LmskdffkOrritBZfGyl3r7nVBRY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP395891.RA4YRDmvPBZ9JU2XY2LmskdffkOrritBZfGyl3r7nVBRY130_provenance.
- NP395891.RA4YRDmvPBZ9JU2XY2LmskdffkOrritBZfGyl3r7nVBRY130_assertion description "[We have identified previously uncharacterized NHP2 mutations that can cause autosomal recessive dyskeratosis congenita but have not found any GAR1 mutations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP395891.RA4YRDmvPBZ9JU2XY2LmskdffkOrritBZfGyl3r7nVBRY130_provenance.
- NP395891.RA4YRDmvPBZ9JU2XY2LmskdffkOrritBZfGyl3r7nVBRY130_assertion evidence source_evidence_literature NP395891.RA4YRDmvPBZ9JU2XY2LmskdffkOrritBZfGyl3r7nVBRY130_provenance.
- NP395891.RA4YRDmvPBZ9JU2XY2LmskdffkOrritBZfGyl3r7nVBRY130_assertion SIO_000772 18523010 NP395891.RA4YRDmvPBZ9JU2XY2LmskdffkOrritBZfGyl3r7nVBRY130_provenance.
- NP395891.RA4YRDmvPBZ9JU2XY2LmskdffkOrritBZfGyl3r7nVBRY130_assertion wasDerivedFrom befree-20140225 NP395891.RA4YRDmvPBZ9JU2XY2LmskdffkOrritBZfGyl3r7nVBRY130_provenance.
- NP395891.RA4YRDmvPBZ9JU2XY2LmskdffkOrritBZfGyl3r7nVBRY130_assertion wasGeneratedBy ECO_0000203 NP395891.RA4YRDmvPBZ9JU2XY2LmskdffkOrritBZfGyl3r7nVBRY130_provenance.
- befree-20140225 importedOn "2014-02-25" NP395891.RA4YRDmvPBZ9JU2XY2LmskdffkOrritBZfGyl3r7nVBRY130_provenance.