Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1216153.RAtZWR1_uGEa_kk2ux4mKX3NPlZhJA2QG4RzLSqGGIXyU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1216153.RAtZWR1_uGEa_kk2ux4mKX3NPlZhJA2QG4RzLSqGGIXyU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1216153.RAtZWR1_uGEa_kk2ux4mKX3NPlZhJA2QG4RzLSqGGIXyU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1216153.RAtZWR1_uGEa_kk2ux4mKX3NPlZhJA2QG4RzLSqGGIXyU130_provenance.
- NP1216153.RAtZWR1_uGEa_kk2ux4mKX3NPlZhJA2QG4RzLSqGGIXyU130_assertion description "[A three-nucleotide in frame deletion was identified in the NPVF gene (p.I71_K72), with a smaller proportion in the CPP (5%) compared to the nIHH (15%) group (P = 0.06).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1216153.RAtZWR1_uGEa_kk2ux4mKX3NPlZhJA2QG4RzLSqGGIXyU130_provenance.
- NP1216153.RAtZWR1_uGEa_kk2ux4mKX3NPlZhJA2QG4RzLSqGGIXyU130_assertion evidence source_evidence_literature NP1216153.RAtZWR1_uGEa_kk2ux4mKX3NPlZhJA2QG4RzLSqGGIXyU130_provenance.
- NP1216153.RAtZWR1_uGEa_kk2ux4mKX3NPlZhJA2QG4RzLSqGGIXyU130_assertion SIO_000772 25180599 NP1216153.RAtZWR1_uGEa_kk2ux4mKX3NPlZhJA2QG4RzLSqGGIXyU130_provenance.
- NP1216153.RAtZWR1_uGEa_kk2ux4mKX3NPlZhJA2QG4RzLSqGGIXyU130_assertion wasDerivedFrom befree-2016 NP1216153.RAtZWR1_uGEa_kk2ux4mKX3NPlZhJA2QG4RzLSqGGIXyU130_provenance.
- NP1216153.RAtZWR1_uGEa_kk2ux4mKX3NPlZhJA2QG4RzLSqGGIXyU130_assertion wasGeneratedBy ECO_0000203 NP1216153.RAtZWR1_uGEa_kk2ux4mKX3NPlZhJA2QG4RzLSqGGIXyU130_provenance.
- befree-2016 importedOn "2016-02-19" NP1216153.RAtZWR1_uGEa_kk2ux4mKX3NPlZhJA2QG4RzLSqGGIXyU130_provenance.