Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP391101.RAN4WY_tT2cdzbAD2CEAYTcXy2XBHd2zpeCcewmS-o0sk130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP391101.RAN4WY_tT2cdzbAD2CEAYTcXy2XBHd2zpeCcewmS-o0sk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP391101.RAN4WY_tT2cdzbAD2CEAYTcXy2XBHd2zpeCcewmS-o0sk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP391101.RAN4WY_tT2cdzbAD2CEAYTcXy2XBHd2zpeCcewmS-o0sk130_provenance.
- NP391101.RAN4WY_tT2cdzbAD2CEAYTcXy2XBHd2zpeCcewmS-o0sk130_assertion description "[No functionally significant mutation was identified, suggesting that APXL is not directly involved in OA1.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP391101.RAN4WY_tT2cdzbAD2CEAYTcXy2XBHd2zpeCcewmS-o0sk130_provenance.
- NP391101.RAN4WY_tT2cdzbAD2CEAYTcXy2XBHd2zpeCcewmS-o0sk130_assertion evidence source_evidence_literature NP391101.RAN4WY_tT2cdzbAD2CEAYTcXy2XBHd2zpeCcewmS-o0sk130_provenance.
- NP391101.RAN4WY_tT2cdzbAD2CEAYTcXy2XBHd2zpeCcewmS-o0sk130_assertion SIO_000772 7795590 NP391101.RAN4WY_tT2cdzbAD2CEAYTcXy2XBHd2zpeCcewmS-o0sk130_provenance.
- NP391101.RAN4WY_tT2cdzbAD2CEAYTcXy2XBHd2zpeCcewmS-o0sk130_assertion wasDerivedFrom befree-20140225 NP391101.RAN4WY_tT2cdzbAD2CEAYTcXy2XBHd2zpeCcewmS-o0sk130_provenance.
- NP391101.RAN4WY_tT2cdzbAD2CEAYTcXy2XBHd2zpeCcewmS-o0sk130_assertion wasGeneratedBy ECO_0000203 NP391101.RAN4WY_tT2cdzbAD2CEAYTcXy2XBHd2zpeCcewmS-o0sk130_provenance.
- befree-20140225 importedOn "2014-02-25" NP391101.RAN4WY_tT2cdzbAD2CEAYTcXy2XBHd2zpeCcewmS-o0sk130_provenance.