Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP791311.RAOCQRHA8Q0QHjstNRCMe3jOkKrix5O4HGnmc_V11escw130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP791311.RAOCQRHA8Q0QHjstNRCMe3jOkKrix5O4HGnmc_V11escw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP791311.RAOCQRHA8Q0QHjstNRCMe3jOkKrix5O4HGnmc_V11escw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP791311.RAOCQRHA8Q0QHjstNRCMe3jOkKrix5O4HGnmc_V11escw130_provenance.
- NP791311.RAOCQRHA8Q0QHjstNRCMe3jOkKrix5O4HGnmc_V11escw130_assertion description "[Losses of 4p11-p13/p15 and 4q occurred in combination in four out of five SM with detectable chromosomal changes, but neither was found in any of the other tumours.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP791311.RAOCQRHA8Q0QHjstNRCMe3jOkKrix5O4HGnmc_V11escw130_provenance.
- NP791311.RAOCQRHA8Q0QHjstNRCMe3jOkKrix5O4HGnmc_V11escw130_assertion evidence source_evidence_literature NP791311.RAOCQRHA8Q0QHjstNRCMe3jOkKrix5O4HGnmc_V11escw130_provenance.
- NP791311.RAOCQRHA8Q0QHjstNRCMe3jOkKrix5O4HGnmc_V11escw130_assertion SIO_000772 16170537 NP791311.RAOCQRHA8Q0QHjstNRCMe3jOkKrix5O4HGnmc_V11escw130_provenance.
- NP791311.RAOCQRHA8Q0QHjstNRCMe3jOkKrix5O4HGnmc_V11escw130_assertion wasDerivedFrom befree-20140225 NP791311.RAOCQRHA8Q0QHjstNRCMe3jOkKrix5O4HGnmc_V11escw130_provenance.
- NP791311.RAOCQRHA8Q0QHjstNRCMe3jOkKrix5O4HGnmc_V11escw130_assertion wasGeneratedBy ECO_0000203 NP791311.RAOCQRHA8Q0QHjstNRCMe3jOkKrix5O4HGnmc_V11escw130_provenance.
- befree-20140225 importedOn "2014-02-25" NP791311.RAOCQRHA8Q0QHjstNRCMe3jOkKrix5O4HGnmc_V11escw130_provenance.