Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP357748.RA4R3vsi7VroNWPjaoY0NTcgTWtWrciPz2eV5RLyMaWIA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP357748.RA4R3vsi7VroNWPjaoY0NTcgTWtWrciPz2eV5RLyMaWIA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP357748.RA4R3vsi7VroNWPjaoY0NTcgTWtWrciPz2eV5RLyMaWIA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP357748.RA4R3vsi7VroNWPjaoY0NTcgTWtWrciPz2eV5RLyMaWIA130_provenance.
- NP357748.RA4R3vsi7VroNWPjaoY0NTcgTWtWrciPz2eV5RLyMaWIA130_assertion description "[In all cases, the pathologic diagnoses were easily resolved: two cases were partial moles (triploid, p57 positive), two cases were early complete moles (diploid, p57 negative), and two cases were twin gestations with normal villi (diploid, p57 positive) admixed with villi from a complete hydatidiform mole (diploid, p57 negative).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP357748.RA4R3vsi7VroNWPjaoY0NTcgTWtWrciPz2eV5RLyMaWIA130_provenance.
- NP357748.RA4R3vsi7VroNWPjaoY0NTcgTWtWrciPz2eV5RLyMaWIA130_assertion evidence source_evidence_literature NP357748.RA4R3vsi7VroNWPjaoY0NTcgTWtWrciPz2eV5RLyMaWIA130_provenance.
- NP357748.RA4R3vsi7VroNWPjaoY0NTcgTWtWrciPz2eV5RLyMaWIA130_assertion SIO_000772 12063872 NP357748.RA4R3vsi7VroNWPjaoY0NTcgTWtWrciPz2eV5RLyMaWIA130_provenance.
- NP357748.RA4R3vsi7VroNWPjaoY0NTcgTWtWrciPz2eV5RLyMaWIA130_assertion wasDerivedFrom befree-2016 NP357748.RA4R3vsi7VroNWPjaoY0NTcgTWtWrciPz2eV5RLyMaWIA130_provenance.
- NP357748.RA4R3vsi7VroNWPjaoY0NTcgTWtWrciPz2eV5RLyMaWIA130_assertion wasGeneratedBy ECO_0000203 NP357748.RA4R3vsi7VroNWPjaoY0NTcgTWtWrciPz2eV5RLyMaWIA130_provenance.
- befree-2016 importedOn "2016-02-19" NP357748.RA4R3vsi7VroNWPjaoY0NTcgTWtWrciPz2eV5RLyMaWIA130_provenance.