Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP914235.RAIcLSNh3RzwEYQQ3mnV9fT6gGINSXqfP8i67KL9SvNHg130_assertion> ?p ?o ?g. }
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- NP914235.RAIcLSNh3RzwEYQQ3mnV9fT6gGINSXqfP8i67KL9SvNHg130_assertion type Assertion NP914235.RAIcLSNh3RzwEYQQ3mnV9fT6gGINSXqfP8i67KL9SvNHg130_head.
- NP914235.RAIcLSNh3RzwEYQQ3mnV9fT6gGINSXqfP8i67KL9SvNHg130_assertion description "[It is suggested that a similar enquiry into the mechanisms of chromosomal deletions in P-MDS is required in order to delineate the role of these abnormalities in the clonal evolution of this group of diseases.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP914235.RAIcLSNh3RzwEYQQ3mnV9fT6gGINSXqfP8i67KL9SvNHg130_provenance.
- NP914235.RAIcLSNh3RzwEYQQ3mnV9fT6gGINSXqfP8i67KL9SvNHg130_assertion evidence source_evidence_literature NP914235.RAIcLSNh3RzwEYQQ3mnV9fT6gGINSXqfP8i67KL9SvNHg130_provenance.
- NP914235.RAIcLSNh3RzwEYQQ3mnV9fT6gGINSXqfP8i67KL9SvNHg130_assertion SIO_000772 1732667 NP914235.RAIcLSNh3RzwEYQQ3mnV9fT6gGINSXqfP8i67KL9SvNHg130_provenance.
- NP914235.RAIcLSNh3RzwEYQQ3mnV9fT6gGINSXqfP8i67KL9SvNHg130_assertion wasDerivedFrom befree-20150227 NP914235.RAIcLSNh3RzwEYQQ3mnV9fT6gGINSXqfP8i67KL9SvNHg130_provenance.
- NP914235.RAIcLSNh3RzwEYQQ3mnV9fT6gGINSXqfP8i67KL9SvNHg130_assertion wasGeneratedBy ECO_0000203 NP914235.RAIcLSNh3RzwEYQQ3mnV9fT6gGINSXqfP8i67KL9SvNHg130_provenance.