Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP191252.RARQAQp_Jp1l02uh7Z1JqeJiEhdZ0RS8PtXebxjPxdBCE130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP191252.RARQAQp_Jp1l02uh7Z1JqeJiEhdZ0RS8PtXebxjPxdBCE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP191252.RARQAQp_Jp1l02uh7Z1JqeJiEhdZ0RS8PtXebxjPxdBCE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP191252.RARQAQp_Jp1l02uh7Z1JqeJiEhdZ0RS8PtXebxjPxdBCE130_provenance.
- NP191252.RARQAQp_Jp1l02uh7Z1JqeJiEhdZ0RS8PtXebxjPxdBCE130_assertion description "[Here we describe a series of novel point mutations in ATRX detected in archival DNA samples from marrow and/or blood of patients with ATMDS by use of denaturing high-performance liquid chromatography (DHPLC), a technique sensitive to low-level mosaicism.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP191252.RARQAQp_Jp1l02uh7Z1JqeJiEhdZ0RS8PtXebxjPxdBCE130_provenance.
- NP191252.RARQAQp_Jp1l02uh7Z1JqeJiEhdZ0RS8PtXebxjPxdBCE130_assertion evidence source_evidence_literature NP191252.RARQAQp_Jp1l02uh7Z1JqeJiEhdZ0RS8PtXebxjPxdBCE130_provenance.
- NP191252.RARQAQp_Jp1l02uh7Z1JqeJiEhdZ0RS8PtXebxjPxdBCE130_assertion SIO_000772 14592816 NP191252.RARQAQp_Jp1l02uh7Z1JqeJiEhdZ0RS8PtXebxjPxdBCE130_provenance.
- NP191252.RARQAQp_Jp1l02uh7Z1JqeJiEhdZ0RS8PtXebxjPxdBCE130_assertion wasDerivedFrom befree-20140225 NP191252.RARQAQp_Jp1l02uh7Z1JqeJiEhdZ0RS8PtXebxjPxdBCE130_provenance.
- NP191252.RARQAQp_Jp1l02uh7Z1JqeJiEhdZ0RS8PtXebxjPxdBCE130_assertion wasGeneratedBy ECO_0000203 NP191252.RARQAQp_Jp1l02uh7Z1JqeJiEhdZ0RS8PtXebxjPxdBCE130_provenance.
- befree-20140225 importedOn "2014-02-25" NP191252.RARQAQp_Jp1l02uh7Z1JqeJiEhdZ0RS8PtXebxjPxdBCE130_provenance.