Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP164030.RADmPaBK8s-e_MyJM29rVHzAvNAzkobQqoaFmI3mQfmmI130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP164030.RADmPaBK8s-e_MyJM29rVHzAvNAzkobQqoaFmI3mQfmmI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP164030.RADmPaBK8s-e_MyJM29rVHzAvNAzkobQqoaFmI3mQfmmI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP164030.RADmPaBK8s-e_MyJM29rVHzAvNAzkobQqoaFmI3mQfmmI130_provenance.
- NP164030.RADmPaBK8s-e_MyJM29rVHzAvNAzkobQqoaFmI3mQfmmI130_assertion description "[Autosomal dominantly inherited missense mutations in lamins A and C cause familial partial lipodystrophy of the Dunnigan-type (FPLD), and myopathies including Emery-Dreifuss muscular dystrophy (EDMD).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP164030.RADmPaBK8s-e_MyJM29rVHzAvNAzkobQqoaFmI3mQfmmI130_provenance.
- NP164030.RADmPaBK8s-e_MyJM29rVHzAvNAzkobQqoaFmI3mQfmmI130_assertion evidence source_evidence_literature NP164030.RADmPaBK8s-e_MyJM29rVHzAvNAzkobQqoaFmI3mQfmmI130_provenance.
- NP164030.RADmPaBK8s-e_MyJM29rVHzAvNAzkobQqoaFmI3mQfmmI130_assertion SIO_000772 12490190 NP164030.RADmPaBK8s-e_MyJM29rVHzAvNAzkobQqoaFmI3mQfmmI130_provenance.
- NP164030.RADmPaBK8s-e_MyJM29rVHzAvNAzkobQqoaFmI3mQfmmI130_assertion wasDerivedFrom befree-20140225 NP164030.RADmPaBK8s-e_MyJM29rVHzAvNAzkobQqoaFmI3mQfmmI130_provenance.
- NP164030.RADmPaBK8s-e_MyJM29rVHzAvNAzkobQqoaFmI3mQfmmI130_assertion wasGeneratedBy ECO_0000203 NP164030.RADmPaBK8s-e_MyJM29rVHzAvNAzkobQqoaFmI3mQfmmI130_provenance.
- befree-20140225 importedOn "2014-02-25" NP164030.RADmPaBK8s-e_MyJM29rVHzAvNAzkobQqoaFmI3mQfmmI130_provenance.