Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP419049.RAG16jExYPgTpBzYLu36cpLCsaOF4VrPqxh6Jsb3Gf8po130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP419049.RAG16jExYPgTpBzYLu36cpLCsaOF4VrPqxh6Jsb3Gf8po130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP419049.RAG16jExYPgTpBzYLu36cpLCsaOF4VrPqxh6Jsb3Gf8po130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP419049.RAG16jExYPgTpBzYLu36cpLCsaOF4VrPqxh6Jsb3Gf8po130_provenance.
- NP419049.RAG16jExYPgTpBzYLu36cpLCsaOF4VrPqxh6Jsb3Gf8po130_assertion description "[Presence or absence of mutation in PHOX2A gene in two siblings with exotropia and recessive CFEOM.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP419049.RAG16jExYPgTpBzYLu36cpLCsaOF4VrPqxh6Jsb3Gf8po130_provenance.
- NP419049.RAG16jExYPgTpBzYLu36cpLCsaOF4VrPqxh6Jsb3Gf8po130_assertion evidence source_evidence_literature NP419049.RAG16jExYPgTpBzYLu36cpLCsaOF4VrPqxh6Jsb3Gf8po130_provenance.
- NP419049.RAG16jExYPgTpBzYLu36cpLCsaOF4VrPqxh6Jsb3Gf8po130_assertion SIO_000772 14597037 NP419049.RAG16jExYPgTpBzYLu36cpLCsaOF4VrPqxh6Jsb3Gf8po130_provenance.
- NP419049.RAG16jExYPgTpBzYLu36cpLCsaOF4VrPqxh6Jsb3Gf8po130_assertion wasDerivedFrom befree-2016 NP419049.RAG16jExYPgTpBzYLu36cpLCsaOF4VrPqxh6Jsb3Gf8po130_provenance.
- NP419049.RAG16jExYPgTpBzYLu36cpLCsaOF4VrPqxh6Jsb3Gf8po130_assertion wasGeneratedBy ECO_0000203 NP419049.RAG16jExYPgTpBzYLu36cpLCsaOF4VrPqxh6Jsb3Gf8po130_provenance.
- befree-2016 importedOn "2016-02-19" NP419049.RAG16jExYPgTpBzYLu36cpLCsaOF4VrPqxh6Jsb3Gf8po130_provenance.