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- source_evidence_literature type ECO_0000212 NP284902.RAxYk4kgQFgCuAA-WTsWvxlcURfV-0_wjBgPy4JBACMSA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP284902.RAxYk4kgQFgCuAA-WTsWvxlcURfV-0_wjBgPy4JBACMSA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP284902.RAxYk4kgQFgCuAA-WTsWvxlcURfV-0_wjBgPy4JBACMSA130_provenance.
- NP284902.RAxYk4kgQFgCuAA-WTsWvxlcURfV-0_wjBgPy4JBACMSA130_assertion description "[We propose MYH10 detection as a new and simple tool to identify inherited platelet disorders and myeloid neoplasms with abnormalities in RUNX1 and its associated proteins.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP284902.RAxYk4kgQFgCuAA-WTsWvxlcURfV-0_wjBgPy4JBACMSA130_provenance.
- NP284902.RAxYk4kgQFgCuAA-WTsWvxlcURfV-0_wjBgPy4JBACMSA130_assertion evidence source_evidence_literature NP284902.RAxYk4kgQFgCuAA-WTsWvxlcURfV-0_wjBgPy4JBACMSA130_provenance.
- NP284902.RAxYk4kgQFgCuAA-WTsWvxlcURfV-0_wjBgPy4JBACMSA130_assertion SIO_000772 22677128 NP284902.RAxYk4kgQFgCuAA-WTsWvxlcURfV-0_wjBgPy4JBACMSA130_provenance.
- NP284902.RAxYk4kgQFgCuAA-WTsWvxlcURfV-0_wjBgPy4JBACMSA130_assertion wasDerivedFrom befree-20150227 NP284902.RAxYk4kgQFgCuAA-WTsWvxlcURfV-0_wjBgPy4JBACMSA130_provenance.
- NP284902.RAxYk4kgQFgCuAA-WTsWvxlcURfV-0_wjBgPy4JBACMSA130_assertion wasGeneratedBy ECO_0000203 NP284902.RAxYk4kgQFgCuAA-WTsWvxlcURfV-0_wjBgPy4JBACMSA130_provenance.
- befree-20150227 importedOn "2015-02-27" NP284902.RAxYk4kgQFgCuAA-WTsWvxlcURfV-0_wjBgPy4JBACMSA130_provenance.