Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP899896.RAuSEOUlrU6ThzfWrVxHbb9zU5fWAqka356EwU8s5EDgI130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP899896.RAuSEOUlrU6ThzfWrVxHbb9zU5fWAqka356EwU8s5EDgI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP899896.RAuSEOUlrU6ThzfWrVxHbb9zU5fWAqka356EwU8s5EDgI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP899896.RAuSEOUlrU6ThzfWrVxHbb9zU5fWAqka356EwU8s5EDgI130_provenance.
- NP899896.RAuSEOUlrU6ThzfWrVxHbb9zU5fWAqka356EwU8s5EDgI130_assertion description "[Multiple osteochondromas (MO) is an autosomal dominant hereditary disorder caused by heterozygous germline mutations in the exostonsin-1 (EXT1) or exostosin-2 (EXT2) genes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP899896.RAuSEOUlrU6ThzfWrVxHbb9zU5fWAqka356EwU8s5EDgI130_provenance.
- NP899896.RAuSEOUlrU6ThzfWrVxHbb9zU5fWAqka356EwU8s5EDgI130_assertion evidence source_evidence_literature NP899896.RAuSEOUlrU6ThzfWrVxHbb9zU5fWAqka356EwU8s5EDgI130_provenance.
- NP899896.RAuSEOUlrU6ThzfWrVxHbb9zU5fWAqka356EwU8s5EDgI130_assertion SIO_000772 23629877 NP899896.RAuSEOUlrU6ThzfWrVxHbb9zU5fWAqka356EwU8s5EDgI130_provenance.
- NP899896.RAuSEOUlrU6ThzfWrVxHbb9zU5fWAqka356EwU8s5EDgI130_assertion wasDerivedFrom befree-20140225 NP899896.RAuSEOUlrU6ThzfWrVxHbb9zU5fWAqka356EwU8s5EDgI130_provenance.
- NP899896.RAuSEOUlrU6ThzfWrVxHbb9zU5fWAqka356EwU8s5EDgI130_assertion wasGeneratedBy ECO_0000203 NP899896.RAuSEOUlrU6ThzfWrVxHbb9zU5fWAqka356EwU8s5EDgI130_provenance.
- befree-20140225 importedOn "2014-02-25" NP899896.RAuSEOUlrU6ThzfWrVxHbb9zU5fWAqka356EwU8s5EDgI130_provenance.