Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP767282.RAILbFRvRDDJjnxS4W_ShGDPtf1RD48Crkl-fjjjyJmb8130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP767282.RAILbFRvRDDJjnxS4W_ShGDPtf1RD48Crkl-fjjjyJmb8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP767282.RAILbFRvRDDJjnxS4W_ShGDPtf1RD48Crkl-fjjjyJmb8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP767282.RAILbFRvRDDJjnxS4W_ShGDPtf1RD48Crkl-fjjjyJmb8130_provenance.
- NP767282.RAILbFRvRDDJjnxS4W_ShGDPtf1RD48Crkl-fjjjyJmb8130_assertion description "[C4B-deficient IgA nephropathy patients display a variety of molecular genetic bases for their protein deficiency.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP767282.RAILbFRvRDDJjnxS4W_ShGDPtf1RD48Crkl-fjjjyJmb8130_provenance.
- NP767282.RAILbFRvRDDJjnxS4W_ShGDPtf1RD48Crkl-fjjjyJmb8130_assertion evidence source_evidence_literature NP767282.RAILbFRvRDDJjnxS4W_ShGDPtf1RD48Crkl-fjjjyJmb8130_provenance.
- NP767282.RAILbFRvRDDJjnxS4W_ShGDPtf1RD48Crkl-fjjjyJmb8130_assertion SIO_000772 2573592 NP767282.RAILbFRvRDDJjnxS4W_ShGDPtf1RD48Crkl-fjjjyJmb8130_provenance.
- NP767282.RAILbFRvRDDJjnxS4W_ShGDPtf1RD48Crkl-fjjjyJmb8130_assertion wasDerivedFrom befree-20140225 NP767282.RAILbFRvRDDJjnxS4W_ShGDPtf1RD48Crkl-fjjjyJmb8130_provenance.
- NP767282.RAILbFRvRDDJjnxS4W_ShGDPtf1RD48Crkl-fjjjyJmb8130_assertion wasGeneratedBy ECO_0000203 NP767282.RAILbFRvRDDJjnxS4W_ShGDPtf1RD48Crkl-fjjjyJmb8130_provenance.
- befree-20140225 importedOn "2014-02-25" NP767282.RAILbFRvRDDJjnxS4W_ShGDPtf1RD48Crkl-fjjjyJmb8130_provenance.