Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP605886.RA-q_d64Yy9wcL2ciiz_8VDYegfo4LTe5qh4-HmtSVYT4130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP605886.RA-q_d64Yy9wcL2ciiz_8VDYegfo4LTe5qh4-HmtSVYT4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP605886.RA-q_d64Yy9wcL2ciiz_8VDYegfo4LTe5qh4-HmtSVYT4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP605886.RA-q_d64Yy9wcL2ciiz_8VDYegfo4LTe5qh4-HmtSVYT4130_provenance.
- NP605886.RA-q_d64Yy9wcL2ciiz_8VDYegfo4LTe5qh4-HmtSVYT4130_assertion description "[Nearly one-fifth of AA patients harbor mutations in genes typically seen in myeloid malignancies that predicted for later transformation to MDS.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP605886.RA-q_d64Yy9wcL2ciiz_8VDYegfo4LTe5qh4-HmtSVYT4130_provenance.
- NP605886.RA-q_d64Yy9wcL2ciiz_8VDYegfo4LTe5qh4-HmtSVYT4130_assertion evidence source_evidence_literature NP605886.RA-q_d64Yy9wcL2ciiz_8VDYegfo4LTe5qh4-HmtSVYT4130_provenance.
- NP605886.RA-q_d64Yy9wcL2ciiz_8VDYegfo4LTe5qh4-HmtSVYT4130_assertion SIO_000772 25139356 NP605886.RA-q_d64Yy9wcL2ciiz_8VDYegfo4LTe5qh4-HmtSVYT4130_provenance.
- NP605886.RA-q_d64Yy9wcL2ciiz_8VDYegfo4LTe5qh4-HmtSVYT4130_assertion wasDerivedFrom befree-20150227 NP605886.RA-q_d64Yy9wcL2ciiz_8VDYegfo4LTe5qh4-HmtSVYT4130_provenance.
- NP605886.RA-q_d64Yy9wcL2ciiz_8VDYegfo4LTe5qh4-HmtSVYT4130_assertion wasGeneratedBy ECO_0000203 NP605886.RA-q_d64Yy9wcL2ciiz_8VDYegfo4LTe5qh4-HmtSVYT4130_provenance.
- befree-20150227 importedOn "2015-02-27" NP605886.RA-q_d64Yy9wcL2ciiz_8VDYegfo4LTe5qh4-HmtSVYT4130_provenance.