Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP136225.RAtgB91XR_WUS5pn68AufxS0Gae3BYkTttMdVMBV85Wfo130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP136225.RAtgB91XR_WUS5pn68AufxS0Gae3BYkTttMdVMBV85Wfo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP136225.RAtgB91XR_WUS5pn68AufxS0Gae3BYkTttMdVMBV85Wfo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP136225.RAtgB91XR_WUS5pn68AufxS0Gae3BYkTttMdVMBV85Wfo130_provenance.
- NP136225.RAtgB91XR_WUS5pn68AufxS0Gae3BYkTttMdVMBV85Wfo130_assertion description "[our data suggest a genetic and functional association of PBX1 with BMD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP136225.RAtgB91XR_WUS5pn68AufxS0Gae3BYkTttMdVMBV85Wfo130_provenance.
- NP136225.RAtgB91XR_WUS5pn68AufxS0Gae3BYkTttMdVMBV85Wfo130_assertion evidence source_evidence_literature NP136225.RAtgB91XR_WUS5pn68AufxS0Gae3BYkTttMdVMBV85Wfo130_provenance.
- NP136225.RAtgB91XR_WUS5pn68AufxS0Gae3BYkTttMdVMBV85Wfo130_assertion SIO_000772 19064610 NP136225.RAtgB91XR_WUS5pn68AufxS0Gae3BYkTttMdVMBV85Wfo130_provenance.
- NP136225.RAtgB91XR_WUS5pn68AufxS0Gae3BYkTttMdVMBV85Wfo130_assertion wasDerivedFrom gad-20150221 NP136225.RAtgB91XR_WUS5pn68AufxS0Gae3BYkTttMdVMBV85Wfo130_provenance.
- NP136225.RAtgB91XR_WUS5pn68AufxS0Gae3BYkTttMdVMBV85Wfo130_assertion wasGeneratedBy ECO_0000203 NP136225.RAtgB91XR_WUS5pn68AufxS0Gae3BYkTttMdVMBV85Wfo130_provenance.
- gad-20150221 importedOn "2015-02-21" NP136225.RAtgB91XR_WUS5pn68AufxS0Gae3BYkTttMdVMBV85Wfo130_provenance.