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- source_evidence_literature type ECO_0000212 NP583468.RANcRm5m6BaBs0c6ss0nrQVK59IcR0sM-FsAtnyeU8vCo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP583468.RANcRm5m6BaBs0c6ss0nrQVK59IcR0sM-FsAtnyeU8vCo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP583468.RANcRm5m6BaBs0c6ss0nrQVK59IcR0sM-FsAtnyeU8vCo130_provenance.
- NP583468.RANcRm5m6BaBs0c6ss0nrQVK59IcR0sM-FsAtnyeU8vCo130_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." NP583468.RANcRm5m6BaBs0c6ss0nrQVK59IcR0sM-FsAtnyeU8vCo130_provenance.
- NP583468.RANcRm5m6BaBs0c6ss0nrQVK59IcR0sM-FsAtnyeU8vCo130_assertion evidence source_evidence_literature NP583468.RANcRm5m6BaBs0c6ss0nrQVK59IcR0sM-FsAtnyeU8vCo130_provenance.
- NP583468.RANcRm5m6BaBs0c6ss0nrQVK59IcR0sM-FsAtnyeU8vCo130_assertion SIO_000772 18923054 NP583468.RANcRm5m6BaBs0c6ss0nrQVK59IcR0sM-FsAtnyeU8vCo130_provenance.
- NP583468.RANcRm5m6BaBs0c6ss0nrQVK59IcR0sM-FsAtnyeU8vCo130_assertion wasDerivedFrom befree-20150227 NP583468.RANcRm5m6BaBs0c6ss0nrQVK59IcR0sM-FsAtnyeU8vCo130_provenance.
- NP583468.RANcRm5m6BaBs0c6ss0nrQVK59IcR0sM-FsAtnyeU8vCo130_assertion wasGeneratedBy ECO_0000203 NP583468.RANcRm5m6BaBs0c6ss0nrQVK59IcR0sM-FsAtnyeU8vCo130_provenance.
- befree-20150227 importedOn "2015-02-27" NP583468.RANcRm5m6BaBs0c6ss0nrQVK59IcR0sM-FsAtnyeU8vCo130_provenance.