Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP242795.RA3Wn_kpzQ4kFid4h_hvU_1o7d5P3wtb-e3x2i6TMtkIM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP242795.RA3Wn_kpzQ4kFid4h_hvU_1o7d5P3wtb-e3x2i6TMtkIM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP242795.RA3Wn_kpzQ4kFid4h_hvU_1o7d5P3wtb-e3x2i6TMtkIM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP242795.RA3Wn_kpzQ4kFid4h_hvU_1o7d5P3wtb-e3x2i6TMtkIM130_provenance.
- NP242795.RA3Wn_kpzQ4kFid4h_hvU_1o7d5P3wtb-e3x2i6TMtkIM130_assertion description "[Results describe the characteristic features of myosclerosis myopathy with a homozygous collagen type 6A2 mutation responsible for a peculiar pattern of collagen VI defects.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP242795.RA3Wn_kpzQ4kFid4h_hvU_1o7d5P3wtb-e3x2i6TMtkIM130_provenance.
- NP242795.RA3Wn_kpzQ4kFid4h_hvU_1o7d5P3wtb-e3x2i6TMtkIM130_assertion evidence source_evidence_literature NP242795.RA3Wn_kpzQ4kFid4h_hvU_1o7d5P3wtb-e3x2i6TMtkIM130_provenance.
- NP242795.RA3Wn_kpzQ4kFid4h_hvU_1o7d5P3wtb-e3x2i6TMtkIM130_assertion SIO_000772 18852439 NP242795.RA3Wn_kpzQ4kFid4h_hvU_1o7d5P3wtb-e3x2i6TMtkIM130_provenance.
- NP242795.RA3Wn_kpzQ4kFid4h_hvU_1o7d5P3wtb-e3x2i6TMtkIM130_assertion wasDerivedFrom lhgdn-20090331 NP242795.RA3Wn_kpzQ4kFid4h_hvU_1o7d5P3wtb-e3x2i6TMtkIM130_provenance.
- NP242795.RA3Wn_kpzQ4kFid4h_hvU_1o7d5P3wtb-e3x2i6TMtkIM130_assertion wasGeneratedBy ECO_0000203 NP242795.RA3Wn_kpzQ4kFid4h_hvU_1o7d5P3wtb-e3x2i6TMtkIM130_provenance.
- lhgdn-20090331 importedOn "2009-03-31" NP242795.RA3Wn_kpzQ4kFid4h_hvU_1o7d5P3wtb-e3x2i6TMtkIM130_provenance.