Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP380849.RA1nCW7mnrvjIG8FlhRizmDhdrRTiwQW0DhtOKItXEp_M130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP380849.RA1nCW7mnrvjIG8FlhRizmDhdrRTiwQW0DhtOKItXEp_M130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP380849.RA1nCW7mnrvjIG8FlhRizmDhdrRTiwQW0DhtOKItXEp_M130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP380849.RA1nCW7mnrvjIG8FlhRizmDhdrRTiwQW0DhtOKItXEp_M130_provenance.
- NP380849.RA1nCW7mnrvjIG8FlhRizmDhdrRTiwQW0DhtOKItXEp_M130_assertion description "[Previously, a genome scan of 98 families affected by SLI was completed by the SLI Consortium, resulting in the identification of two quantitative trait loci (QTL) on chromosomes 16q (SLI1) and 19q (SLI2).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP380849.RA1nCW7mnrvjIG8FlhRizmDhdrRTiwQW0DhtOKItXEp_M130_provenance.
- NP380849.RA1nCW7mnrvjIG8FlhRizmDhdrRTiwQW0DhtOKItXEp_M130_assertion evidence source_evidence_literature NP380849.RA1nCW7mnrvjIG8FlhRizmDhdrRTiwQW0DhtOKItXEp_M130_provenance.
- NP380849.RA1nCW7mnrvjIG8FlhRizmDhdrRTiwQW0DhtOKItXEp_M130_assertion SIO_000772 17388790 NP380849.RA1nCW7mnrvjIG8FlhRizmDhdrRTiwQW0DhtOKItXEp_M130_provenance.
- NP380849.RA1nCW7mnrvjIG8FlhRizmDhdrRTiwQW0DhtOKItXEp_M130_assertion wasDerivedFrom befree-20140225 NP380849.RA1nCW7mnrvjIG8FlhRizmDhdrRTiwQW0DhtOKItXEp_M130_provenance.
- NP380849.RA1nCW7mnrvjIG8FlhRizmDhdrRTiwQW0DhtOKItXEp_M130_assertion wasGeneratedBy ECO_0000203 NP380849.RA1nCW7mnrvjIG8FlhRizmDhdrRTiwQW0DhtOKItXEp_M130_provenance.
- befree-20140225 importedOn "2014-02-25" NP380849.RA1nCW7mnrvjIG8FlhRizmDhdrRTiwQW0DhtOKItXEp_M130_provenance.