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- source_evidence_literature type ECO_0000212 NP285491.RAEt5iFPa9gYAol3Cbib8aXqFG3_XsbeApP5qE0VCp2So130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP285491.RAEt5iFPa9gYAol3Cbib8aXqFG3_XsbeApP5qE0VCp2So130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP285491.RAEt5iFPa9gYAol3Cbib8aXqFG3_XsbeApP5qE0VCp2So130_provenance.
- NP285491.RAEt5iFPa9gYAol3Cbib8aXqFG3_XsbeApP5qE0VCp2So130_assertion description "[We, therefore, investigated individuals from families with one or more first-degree relatives with myelodysplastic syndrome/acute myeloid leukemia with wild-type RUNX1 and CEBPA, for GATA2 mutations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP285491.RAEt5iFPa9gYAol3Cbib8aXqFG3_XsbeApP5qE0VCp2So130_provenance.
- NP285491.RAEt5iFPa9gYAol3Cbib8aXqFG3_XsbeApP5qE0VCp2So130_assertion evidence source_evidence_literature NP285491.RAEt5iFPa9gYAol3Cbib8aXqFG3_XsbeApP5qE0VCp2So130_provenance.
- NP285491.RAEt5iFPa9gYAol3Cbib8aXqFG3_XsbeApP5qE0VCp2So130_assertion SIO_000772 22271902 NP285491.RAEt5iFPa9gYAol3Cbib8aXqFG3_XsbeApP5qE0VCp2So130_provenance.
- NP285491.RAEt5iFPa9gYAol3Cbib8aXqFG3_XsbeApP5qE0VCp2So130_assertion wasDerivedFrom befree-20150227 NP285491.RAEt5iFPa9gYAol3Cbib8aXqFG3_XsbeApP5qE0VCp2So130_provenance.
- NP285491.RAEt5iFPa9gYAol3Cbib8aXqFG3_XsbeApP5qE0VCp2So130_assertion wasGeneratedBy ECO_0000203 NP285491.RAEt5iFPa9gYAol3Cbib8aXqFG3_XsbeApP5qE0VCp2So130_provenance.
- befree-20150227 importedOn "2015-02-27" NP285491.RAEt5iFPa9gYAol3Cbib8aXqFG3_XsbeApP5qE0VCp2So130_provenance.