Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP243681.RAb-qd1x15vw4YrhcrI1Wpk9xfs0TN2ETJwATVfd96SUI130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP243681.RAb-qd1x15vw4YrhcrI1Wpk9xfs0TN2ETJwATVfd96SUI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP243681.RAb-qd1x15vw4YrhcrI1Wpk9xfs0TN2ETJwATVfd96SUI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP243681.RAb-qd1x15vw4YrhcrI1Wpk9xfs0TN2ETJwATVfd96SUI130_provenance.
- NP243681.RAb-qd1x15vw4YrhcrI1Wpk9xfs0TN2ETJwATVfd96SUI130_assertion description "[The commonly deleted region (CDR) for the 5q- syndrome has been identified as a 1.5-megabase interval on human chromosome 5q32.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP243681.RAb-qd1x15vw4YrhcrI1Wpk9xfs0TN2ETJwATVfd96SUI130_provenance.
- NP243681.RAb-qd1x15vw4YrhcrI1Wpk9xfs0TN2ETJwATVfd96SUI130_assertion evidence source_evidence_literature NP243681.RAb-qd1x15vw4YrhcrI1Wpk9xfs0TN2ETJwATVfd96SUI130_provenance.
- NP243681.RAb-qd1x15vw4YrhcrI1Wpk9xfs0TN2ETJwATVfd96SUI130_assertion SIO_000772 17625608 NP243681.RAb-qd1x15vw4YrhcrI1Wpk9xfs0TN2ETJwATVfd96SUI130_provenance.
- NP243681.RAb-qd1x15vw4YrhcrI1Wpk9xfs0TN2ETJwATVfd96SUI130_assertion wasDerivedFrom befree-20140225 NP243681.RAb-qd1x15vw4YrhcrI1Wpk9xfs0TN2ETJwATVfd96SUI130_provenance.
- NP243681.RAb-qd1x15vw4YrhcrI1Wpk9xfs0TN2ETJwATVfd96SUI130_assertion wasGeneratedBy ECO_0000203 NP243681.RAb-qd1x15vw4YrhcrI1Wpk9xfs0TN2ETJwATVfd96SUI130_provenance.
- befree-20140225 importedOn "2014-02-25" NP243681.RAb-qd1x15vw4YrhcrI1Wpk9xfs0TN2ETJwATVfd96SUI130_provenance.