Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP748215.RABmY8BFePjWG3aCQWCdz3ZeMRAVH53NsFbK7VhvR3bHo130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP748215.RABmY8BFePjWG3aCQWCdz3ZeMRAVH53NsFbK7VhvR3bHo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP748215.RABmY8BFePjWG3aCQWCdz3ZeMRAVH53NsFbK7VhvR3bHo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP748215.RABmY8BFePjWG3aCQWCdz3ZeMRAVH53NsFbK7VhvR3bHo130_provenance.
- NP748215.RABmY8BFePjWG3aCQWCdz3ZeMRAVH53NsFbK7VhvR3bHo130_assertion description "[A point mutation in the POU-specific portion of the human gene that encodes the tissue-specific POU-domain transcription factor, Pit-1, results in hypopituitarism, with deficiencies of growth hormone, prolactin, and thyroid-stimulating hormone.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP748215.RABmY8BFePjWG3aCQWCdz3ZeMRAVH53NsFbK7VhvR3bHo130_provenance.
- NP748215.RABmY8BFePjWG3aCQWCdz3ZeMRAVH53NsFbK7VhvR3bHo130_assertion evidence source_evidence_literature NP748215.RABmY8BFePjWG3aCQWCdz3ZeMRAVH53NsFbK7VhvR3bHo130_provenance.
- NP748215.RABmY8BFePjWG3aCQWCdz3ZeMRAVH53NsFbK7VhvR3bHo130_assertion SIO_000772 1509263 NP748215.RABmY8BFePjWG3aCQWCdz3ZeMRAVH53NsFbK7VhvR3bHo130_provenance.
- NP748215.RABmY8BFePjWG3aCQWCdz3ZeMRAVH53NsFbK7VhvR3bHo130_assertion wasDerivedFrom befree-20140225 NP748215.RABmY8BFePjWG3aCQWCdz3ZeMRAVH53NsFbK7VhvR3bHo130_provenance.
- NP748215.RABmY8BFePjWG3aCQWCdz3ZeMRAVH53NsFbK7VhvR3bHo130_assertion wasGeneratedBy ECO_0000203 NP748215.RABmY8BFePjWG3aCQWCdz3ZeMRAVH53NsFbK7VhvR3bHo130_provenance.
- befree-20140225 importedOn "2014-02-25" NP748215.RABmY8BFePjWG3aCQWCdz3ZeMRAVH53NsFbK7VhvR3bHo130_provenance.