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- source_evidence_literature type ECO_0000212 NP698195.RAT2lC0WAnxAeXmx20KPcKRuBmeeF0DBP8ApPmyBVqhGk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP698195.RAT2lC0WAnxAeXmx20KPcKRuBmeeF0DBP8ApPmyBVqhGk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP698195.RAT2lC0WAnxAeXmx20KPcKRuBmeeF0DBP8ApPmyBVqhGk130_provenance.
- NP698195.RAT2lC0WAnxAeXmx20KPcKRuBmeeF0DBP8ApPmyBVqhGk130_assertion description "[Two recently published studies demonstrated a strong association of genetic variants in the gene that encodes the molecular motor protein nonmuscle myosin 2a (MYH9) with ESRD in African American patients without diabetes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP698195.RAT2lC0WAnxAeXmx20KPcKRuBmeeF0DBP8ApPmyBVqhGk130_provenance.
- NP698195.RAT2lC0WAnxAeXmx20KPcKRuBmeeF0DBP8ApPmyBVqhGk130_assertion evidence source_evidence_literature NP698195.RAT2lC0WAnxAeXmx20KPcKRuBmeeF0DBP8ApPmyBVqhGk130_provenance.
- NP698195.RAT2lC0WAnxAeXmx20KPcKRuBmeeF0DBP8ApPmyBVqhGk130_assertion SIO_000772 18923054 NP698195.RAT2lC0WAnxAeXmx20KPcKRuBmeeF0DBP8ApPmyBVqhGk130_provenance.
- NP698195.RAT2lC0WAnxAeXmx20KPcKRuBmeeF0DBP8ApPmyBVqhGk130_assertion wasDerivedFrom befree-2016 NP698195.RAT2lC0WAnxAeXmx20KPcKRuBmeeF0DBP8ApPmyBVqhGk130_provenance.
- NP698195.RAT2lC0WAnxAeXmx20KPcKRuBmeeF0DBP8ApPmyBVqhGk130_assertion wasGeneratedBy ECO_0000203 NP698195.RAT2lC0WAnxAeXmx20KPcKRuBmeeF0DBP8ApPmyBVqhGk130_provenance.
- befree-2016 importedOn "2016-02-19" NP698195.RAT2lC0WAnxAeXmx20KPcKRuBmeeF0DBP8ApPmyBVqhGk130_provenance.