Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP802651.RAfCR-7rUud_oHkPYED8T17qOxW5rEOpgzaPf1fwmD5xI130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP802651.RAfCR-7rUud_oHkPYED8T17qOxW5rEOpgzaPf1fwmD5xI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP802651.RAfCR-7rUud_oHkPYED8T17qOxW5rEOpgzaPf1fwmD5xI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP802651.RAfCR-7rUud_oHkPYED8T17qOxW5rEOpgzaPf1fwmD5xI130_provenance.
- NP802651.RAfCR-7rUud_oHkPYED8T17qOxW5rEOpgzaPf1fwmD5xI130_assertion description "[Absence of mutations in NR2E1 and SNX3 in five patients with MMEP (microcephaly, microphthalmia, ectrodactyly, and prognathism) and related phenotypes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP802651.RAfCR-7rUud_oHkPYED8T17qOxW5rEOpgzaPf1fwmD5xI130_provenance.
- NP802651.RAfCR-7rUud_oHkPYED8T17qOxW5rEOpgzaPf1fwmD5xI130_assertion evidence source_evidence_literature NP802651.RAfCR-7rUud_oHkPYED8T17qOxW5rEOpgzaPf1fwmD5xI130_provenance.
- NP802651.RAfCR-7rUud_oHkPYED8T17qOxW5rEOpgzaPf1fwmD5xI130_assertion SIO_000772 17655765 NP802651.RAfCR-7rUud_oHkPYED8T17qOxW5rEOpgzaPf1fwmD5xI130_provenance.
- NP802651.RAfCR-7rUud_oHkPYED8T17qOxW5rEOpgzaPf1fwmD5xI130_assertion wasDerivedFrom befree-20150227 NP802651.RAfCR-7rUud_oHkPYED8T17qOxW5rEOpgzaPf1fwmD5xI130_provenance.
- NP802651.RAfCR-7rUud_oHkPYED8T17qOxW5rEOpgzaPf1fwmD5xI130_assertion wasGeneratedBy ECO_0000203 NP802651.RAfCR-7rUud_oHkPYED8T17qOxW5rEOpgzaPf1fwmD5xI130_provenance.
- befree-20150227 importedOn "2015-02-27" NP802651.RAfCR-7rUud_oHkPYED8T17qOxW5rEOpgzaPf1fwmD5xI130_provenance.