Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP829628.RAkFu2YGCv7lAVG2dRtQqVFKxTLh2Mi4TDbZPRiz4COs0130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP829628.RAkFu2YGCv7lAVG2dRtQqVFKxTLh2Mi4TDbZPRiz4COs0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP829628.RAkFu2YGCv7lAVG2dRtQqVFKxTLh2Mi4TDbZPRiz4COs0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP829628.RAkFu2YGCv7lAVG2dRtQqVFKxTLh2Mi4TDbZPRiz4COs0130_provenance.
- NP829628.RAkFu2YGCv7lAVG2dRtQqVFKxTLh2Mi4TDbZPRiz4COs0130_assertion description "[In addition, the spectrum of HPRT deletions observed in FA patients differs from that of healthy children: there is a high frequency of 3'-terminal deletions and a strikingly low proportion of V(D)J mediated events.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP829628.RAkFu2YGCv7lAVG2dRtQqVFKxTLh2Mi4TDbZPRiz4COs0130_provenance.
- NP829628.RAkFu2YGCv7lAVG2dRtQqVFKxTLh2Mi4TDbZPRiz4COs0130_assertion evidence source_evidence_literature NP829628.RAkFu2YGCv7lAVG2dRtQqVFKxTLh2Mi4TDbZPRiz4COs0130_provenance.
- NP829628.RAkFu2YGCv7lAVG2dRtQqVFKxTLh2Mi4TDbZPRiz4COs0130_assertion SIO_000772 10635999 NP829628.RAkFu2YGCv7lAVG2dRtQqVFKxTLh2Mi4TDbZPRiz4COs0130_provenance.
- NP829628.RAkFu2YGCv7lAVG2dRtQqVFKxTLh2Mi4TDbZPRiz4COs0130_assertion wasDerivedFrom befree-20140225 NP829628.RAkFu2YGCv7lAVG2dRtQqVFKxTLh2Mi4TDbZPRiz4COs0130_provenance.
- NP829628.RAkFu2YGCv7lAVG2dRtQqVFKxTLh2Mi4TDbZPRiz4COs0130_assertion wasGeneratedBy ECO_0000203 NP829628.RAkFu2YGCv7lAVG2dRtQqVFKxTLh2Mi4TDbZPRiz4COs0130_provenance.
- befree-20140225 importedOn "2014-02-25" NP829628.RAkFu2YGCv7lAVG2dRtQqVFKxTLh2Mi4TDbZPRiz4COs0130_provenance.