Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP924175.RAisl0_4XjMj77HZ6g5Dd6hNqvXisrhDZ0QpnKR3PdqL0130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP924175.RAisl0_4XjMj77HZ6g5Dd6hNqvXisrhDZ0QpnKR3PdqL0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP924175.RAisl0_4XjMj77HZ6g5Dd6hNqvXisrhDZ0QpnKR3PdqL0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP924175.RAisl0_4XjMj77HZ6g5Dd6hNqvXisrhDZ0QpnKR3PdqL0130_provenance.
- NP924175.RAisl0_4XjMj77HZ6g5Dd6hNqvXisrhDZ0QpnKR3PdqL0130_assertion description "[NOTCH1 mutations, found in 63 patients (11%), were associated with unmutated IGHV, high expression of CD38 and ZAP-70, trisomy 12, advanced stage and elevated lactate dehydrogenase.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP924175.RAisl0_4XjMj77HZ6g5Dd6hNqvXisrhDZ0QpnKR3PdqL0130_provenance.
- NP924175.RAisl0_4XjMj77HZ6g5Dd6hNqvXisrhDZ0QpnKR3PdqL0130_assertion evidence source_evidence_literature NP924175.RAisl0_4XjMj77HZ6g5Dd6hNqvXisrhDZ0QpnKR3PdqL0130_provenance.
- NP924175.RAisl0_4XjMj77HZ6g5Dd6hNqvXisrhDZ0QpnKR3PdqL0130_assertion SIO_000772 23295735 NP924175.RAisl0_4XjMj77HZ6g5Dd6hNqvXisrhDZ0QpnKR3PdqL0130_provenance.
- NP924175.RAisl0_4XjMj77HZ6g5Dd6hNqvXisrhDZ0QpnKR3PdqL0130_assertion wasDerivedFrom befree-20140225 NP924175.RAisl0_4XjMj77HZ6g5Dd6hNqvXisrhDZ0QpnKR3PdqL0130_provenance.
- NP924175.RAisl0_4XjMj77HZ6g5Dd6hNqvXisrhDZ0QpnKR3PdqL0130_assertion wasGeneratedBy ECO_0000203 NP924175.RAisl0_4XjMj77HZ6g5Dd6hNqvXisrhDZ0QpnKR3PdqL0130_provenance.
- befree-20140225 importedOn "2014-02-25" NP924175.RAisl0_4XjMj77HZ6g5Dd6hNqvXisrhDZ0QpnKR3PdqL0130_provenance.