Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1016927.RAz7ZkymIAuEC6o-_9CpTR8CsXRkGrZAHGq2K462TWvZs130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1016927.RAz7ZkymIAuEC6o-_9CpTR8CsXRkGrZAHGq2K462TWvZs130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1016927.RAz7ZkymIAuEC6o-_9CpTR8CsXRkGrZAHGq2K462TWvZs130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1016927.RAz7ZkymIAuEC6o-_9CpTR8CsXRkGrZAHGq2K462TWvZs130_provenance.
- NP1016927.RAz7ZkymIAuEC6o-_9CpTR8CsXRkGrZAHGq2K462TWvZs130_assertion description "[Among the prognostically important aberrations, the del13q14 was present in 36 (51.4%), trisomy 12 in 9 (12.8%), del11q22 in 9 (12.8%), and del17p13 in 4 cases (5.7%).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1016927.RAz7ZkymIAuEC6o-_9CpTR8CsXRkGrZAHGq2K462TWvZs130_provenance.
- NP1016927.RAz7ZkymIAuEC6o-_9CpTR8CsXRkGrZAHGq2K462TWvZs130_assertion evidence source_evidence_literature NP1016927.RAz7ZkymIAuEC6o-_9CpTR8CsXRkGrZAHGq2K462TWvZs130_provenance.
- NP1016927.RAz7ZkymIAuEC6o-_9CpTR8CsXRkGrZAHGq2K462TWvZs130_assertion SIO_000772 17053054 NP1016927.RAz7ZkymIAuEC6o-_9CpTR8CsXRkGrZAHGq2K462TWvZs130_provenance.
- NP1016927.RAz7ZkymIAuEC6o-_9CpTR8CsXRkGrZAHGq2K462TWvZs130_assertion wasDerivedFrom befree-20150227 NP1016927.RAz7ZkymIAuEC6o-_9CpTR8CsXRkGrZAHGq2K462TWvZs130_provenance.
- NP1016927.RAz7ZkymIAuEC6o-_9CpTR8CsXRkGrZAHGq2K462TWvZs130_assertion wasGeneratedBy ECO_0000203 NP1016927.RAz7ZkymIAuEC6o-_9CpTR8CsXRkGrZAHGq2K462TWvZs130_provenance.
- befree-20150227 importedOn "2015-02-27" NP1016927.RAz7ZkymIAuEC6o-_9CpTR8CsXRkGrZAHGq2K462TWvZs130_provenance.