Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP845140.RA3D0oof1l54ZBgXeSFAzDLeferG1MxVT43g9elYhf7s0130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP845140.RA3D0oof1l54ZBgXeSFAzDLeferG1MxVT43g9elYhf7s0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP845140.RA3D0oof1l54ZBgXeSFAzDLeferG1MxVT43g9elYhf7s0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP845140.RA3D0oof1l54ZBgXeSFAzDLeferG1MxVT43g9elYhf7s0130_provenance.
- NP845140.RA3D0oof1l54ZBgXeSFAzDLeferG1MxVT43g9elYhf7s0130_assertion description "[Mutations in fibulin-4 (EFEMP2) and fibulin-5 (FBLN5) were described to be causative for autosomal recessive cutis laxa type 1 in a few families each.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP845140.RA3D0oof1l54ZBgXeSFAzDLeferG1MxVT43g9elYhf7s0130_provenance.
- NP845140.RA3D0oof1l54ZBgXeSFAzDLeferG1MxVT43g9elYhf7s0130_assertion evidence source_evidence_literature NP845140.RA3D0oof1l54ZBgXeSFAzDLeferG1MxVT43g9elYhf7s0130_provenance.
- NP845140.RA3D0oof1l54ZBgXeSFAzDLeferG1MxVT43g9elYhf7s0130_assertion SIO_000772 19664000 NP845140.RA3D0oof1l54ZBgXeSFAzDLeferG1MxVT43g9elYhf7s0130_provenance.
- NP845140.RA3D0oof1l54ZBgXeSFAzDLeferG1MxVT43g9elYhf7s0130_assertion wasDerivedFrom befree-20150227 NP845140.RA3D0oof1l54ZBgXeSFAzDLeferG1MxVT43g9elYhf7s0130_provenance.
- NP845140.RA3D0oof1l54ZBgXeSFAzDLeferG1MxVT43g9elYhf7s0130_assertion wasGeneratedBy ECO_0000203 NP845140.RA3D0oof1l54ZBgXeSFAzDLeferG1MxVT43g9elYhf7s0130_provenance.
- befree-20150227 importedOn "2015-02-27" NP845140.RA3D0oof1l54ZBgXeSFAzDLeferG1MxVT43g9elYhf7s0130_provenance.