Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP888250.RA5Z73uD-vFdcqsPAwo2ZyfikkmuRQ65Ouf9NlyizIJbc130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP888250.RA5Z73uD-vFdcqsPAwo2ZyfikkmuRQ65Ouf9NlyizIJbc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP888250.RA5Z73uD-vFdcqsPAwo2ZyfikkmuRQ65Ouf9NlyizIJbc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP888250.RA5Z73uD-vFdcqsPAwo2ZyfikkmuRQ65Ouf9NlyizIJbc130_provenance.
- NP888250.RA5Z73uD-vFdcqsPAwo2ZyfikkmuRQ65Ouf9NlyizIJbc130_assertion description "[The expressed constructs include the intact integrin and two mutants, namely hbeta3(Y747F/Y759F) and hbeta3(S752P), each of which induces the bleeding dyscrasia, Glanzmann's thrombasthenia, in humans.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP888250.RA5Z73uD-vFdcqsPAwo2ZyfikkmuRQ65Ouf9NlyizIJbc130_provenance.
- NP888250.RA5Z73uD-vFdcqsPAwo2ZyfikkmuRQ65Ouf9NlyizIJbc130_assertion evidence source_evidence_literature NP888250.RA5Z73uD-vFdcqsPAwo2ZyfikkmuRQ65Ouf9NlyizIJbc130_provenance.
- NP888250.RA5Z73uD-vFdcqsPAwo2ZyfikkmuRQ65Ouf9NlyizIJbc130_assertion SIO_000772 16294265 NP888250.RA5Z73uD-vFdcqsPAwo2ZyfikkmuRQ65Ouf9NlyizIJbc130_provenance.
- NP888250.RA5Z73uD-vFdcqsPAwo2ZyfikkmuRQ65Ouf9NlyizIJbc130_assertion wasDerivedFrom befree-20140225 NP888250.RA5Z73uD-vFdcqsPAwo2ZyfikkmuRQ65Ouf9NlyizIJbc130_provenance.
- NP888250.RA5Z73uD-vFdcqsPAwo2ZyfikkmuRQ65Ouf9NlyizIJbc130_assertion wasGeneratedBy ECO_0000203 NP888250.RA5Z73uD-vFdcqsPAwo2ZyfikkmuRQ65Ouf9NlyizIJbc130_provenance.
- befree-20140225 importedOn "2014-02-25" NP888250.RA5Z73uD-vFdcqsPAwo2ZyfikkmuRQ65Ouf9NlyizIJbc130_provenance.