Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP238740.RA9d8g2c5gIrbF0i1hQfzTgmQUUAy0fMqHfOUl9rs4tPE130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP238740.RA9d8g2c5gIrbF0i1hQfzTgmQUUAy0fMqHfOUl9rs4tPE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP238740.RA9d8g2c5gIrbF0i1hQfzTgmQUUAy0fMqHfOUl9rs4tPE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP238740.RA9d8g2c5gIrbF0i1hQfzTgmQUUAy0fMqHfOUl9rs4tPE130_provenance.
- NP238740.RA9d8g2c5gIrbF0i1hQfzTgmQUUAy0fMqHfOUl9rs4tPE130_assertion description "[(AC)n microsatellite polymorphism and 14-nucleotide deletion in exon 42 ankyrin-1 gene in several families with hereditary spherocytosis in a population of South-Western Poland.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP238740.RA9d8g2c5gIrbF0i1hQfzTgmQUUAy0fMqHfOUl9rs4tPE130_provenance.
- NP238740.RA9d8g2c5gIrbF0i1hQfzTgmQUUAy0fMqHfOUl9rs4tPE130_assertion evidence source_evidence_literature NP238740.RA9d8g2c5gIrbF0i1hQfzTgmQUUAy0fMqHfOUl9rs4tPE130_provenance.
- NP238740.RA9d8g2c5gIrbF0i1hQfzTgmQUUAy0fMqHfOUl9rs4tPE130_assertion SIO_000772 16518602 NP238740.RA9d8g2c5gIrbF0i1hQfzTgmQUUAy0fMqHfOUl9rs4tPE130_provenance.
- NP238740.RA9d8g2c5gIrbF0i1hQfzTgmQUUAy0fMqHfOUl9rs4tPE130_assertion wasDerivedFrom befree-20150227 NP238740.RA9d8g2c5gIrbF0i1hQfzTgmQUUAy0fMqHfOUl9rs4tPE130_provenance.
- NP238740.RA9d8g2c5gIrbF0i1hQfzTgmQUUAy0fMqHfOUl9rs4tPE130_assertion wasGeneratedBy ECO_0000203 NP238740.RA9d8g2c5gIrbF0i1hQfzTgmQUUAy0fMqHfOUl9rs4tPE130_provenance.
- befree-20150227 importedOn "2015-02-27" NP238740.RA9d8g2c5gIrbF0i1hQfzTgmQUUAy0fMqHfOUl9rs4tPE130_provenance.