Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1065284.RAyjFou8Cw0yBRP64pK86LqPXPbj_2tbVO8KtYWYj86Ko130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1065284.RAyjFou8Cw0yBRP64pK86LqPXPbj_2tbVO8KtYWYj86Ko130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1065284.RAyjFou8Cw0yBRP64pK86LqPXPbj_2tbVO8KtYWYj86Ko130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1065284.RAyjFou8Cw0yBRP64pK86LqPXPbj_2tbVO8KtYWYj86Ko130_provenance.
- NP1065284.RAyjFou8Cw0yBRP64pK86LqPXPbj_2tbVO8KtYWYj86Ko130_assertion description "[Identification of one novel mutation in the C-propeptide of COL2A1 in a Chinese family with spondyloperipheral dysplasia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1065284.RAyjFou8Cw0yBRP64pK86LqPXPbj_2tbVO8KtYWYj86Ko130_provenance.
- NP1065284.RAyjFou8Cw0yBRP64pK86LqPXPbj_2tbVO8KtYWYj86Ko130_assertion evidence source_evidence_literature NP1065284.RAyjFou8Cw0yBRP64pK86LqPXPbj_2tbVO8KtYWYj86Ko130_provenance.
- NP1065284.RAyjFou8Cw0yBRP64pK86LqPXPbj_2tbVO8KtYWYj86Ko130_assertion SIO_000772 23545312 NP1065284.RAyjFou8Cw0yBRP64pK86LqPXPbj_2tbVO8KtYWYj86Ko130_provenance.
- NP1065284.RAyjFou8Cw0yBRP64pK86LqPXPbj_2tbVO8KtYWYj86Ko130_assertion wasDerivedFrom befree-2016 NP1065284.RAyjFou8Cw0yBRP64pK86LqPXPbj_2tbVO8KtYWYj86Ko130_provenance.
- NP1065284.RAyjFou8Cw0yBRP64pK86LqPXPbj_2tbVO8KtYWYj86Ko130_assertion wasGeneratedBy ECO_0000203 NP1065284.RAyjFou8Cw0yBRP64pK86LqPXPbj_2tbVO8KtYWYj86Ko130_provenance.
- befree-2016 importedOn "2016-02-19" NP1065284.RAyjFou8Cw0yBRP64pK86LqPXPbj_2tbVO8KtYWYj86Ko130_provenance.