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- source_evidence_literature type ECO_0000212 NP694802.RAwAYIkmH-rK1WH3nHpEra6l_m8KqMm9sJ6yehF5oAeCc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP694802.RAwAYIkmH-rK1WH3nHpEra6l_m8KqMm9sJ6yehF5oAeCc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP694802.RAwAYIkmH-rK1WH3nHpEra6l_m8KqMm9sJ6yehF5oAeCc130_provenance.
- NP694802.RAwAYIkmH-rK1WH3nHpEra6l_m8KqMm9sJ6yehF5oAeCc130_assertion description "[The most severe HPE types were associated with SIX3 and ZIC2 mutations, whereas microforms were associated with SHH mutations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP694802.RAwAYIkmH-rK1WH3nHpEra6l_m8KqMm9sJ6yehF5oAeCc130_provenance.
- NP694802.RAwAYIkmH-rK1WH3nHpEra6l_m8KqMm9sJ6yehF5oAeCc130_assertion evidence source_evidence_literature NP694802.RAwAYIkmH-rK1WH3nHpEra6l_m8KqMm9sJ6yehF5oAeCc130_provenance.
- NP694802.RAwAYIkmH-rK1WH3nHpEra6l_m8KqMm9sJ6yehF5oAeCc130_assertion SIO_000772 21940735 NP694802.RAwAYIkmH-rK1WH3nHpEra6l_m8KqMm9sJ6yehF5oAeCc130_provenance.
- NP694802.RAwAYIkmH-rK1WH3nHpEra6l_m8KqMm9sJ6yehF5oAeCc130_assertion wasDerivedFrom befree-20150227 NP694802.RAwAYIkmH-rK1WH3nHpEra6l_m8KqMm9sJ6yehF5oAeCc130_provenance.
- NP694802.RAwAYIkmH-rK1WH3nHpEra6l_m8KqMm9sJ6yehF5oAeCc130_assertion wasGeneratedBy ECO_0000203 NP694802.RAwAYIkmH-rK1WH3nHpEra6l_m8KqMm9sJ6yehF5oAeCc130_provenance.
- befree-20150227 importedOn "2015-02-27" NP694802.RAwAYIkmH-rK1WH3nHpEra6l_m8KqMm9sJ6yehF5oAeCc130_provenance.