Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1308042.RA2UDu1DrWssW_r6NMlUr3A-W5ZoHU4ftUqaRWPO8q3_c130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1308042.RA2UDu1DrWssW_r6NMlUr3A-W5ZoHU4ftUqaRWPO8q3_c130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1308042.RA2UDu1DrWssW_r6NMlUr3A-W5ZoHU4ftUqaRWPO8q3_c130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1308042.RA2UDu1DrWssW_r6NMlUr3A-W5ZoHU4ftUqaRWPO8q3_c130_provenance.
- NP1308042.RA2UDu1DrWssW_r6NMlUr3A-W5ZoHU4ftUqaRWPO8q3_c130_assertion description "[An infant with multiple anomalies and developmental delay during his first year was found to have an intersitital deletion of band p14 from the proximal short arm of chromosome 3.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1308042.RA2UDu1DrWssW_r6NMlUr3A-W5ZoHU4ftUqaRWPO8q3_c130_provenance.
- NP1308042.RA2UDu1DrWssW_r6NMlUr3A-W5ZoHU4ftUqaRWPO8q3_c130_assertion evidence source_evidence_literature NP1308042.RA2UDu1DrWssW_r6NMlUr3A-W5ZoHU4ftUqaRWPO8q3_c130_provenance.
- NP1308042.RA2UDu1DrWssW_r6NMlUr3A-W5ZoHU4ftUqaRWPO8q3_c130_assertion SIO_000772 7424912 NP1308042.RA2UDu1DrWssW_r6NMlUr3A-W5ZoHU4ftUqaRWPO8q3_c130_provenance.
- NP1308042.RA2UDu1DrWssW_r6NMlUr3A-W5ZoHU4ftUqaRWPO8q3_c130_assertion wasDerivedFrom befree-2016 NP1308042.RA2UDu1DrWssW_r6NMlUr3A-W5ZoHU4ftUqaRWPO8q3_c130_provenance.
- NP1308042.RA2UDu1DrWssW_r6NMlUr3A-W5ZoHU4ftUqaRWPO8q3_c130_assertion wasGeneratedBy ECO_0000203 NP1308042.RA2UDu1DrWssW_r6NMlUr3A-W5ZoHU4ftUqaRWPO8q3_c130_provenance.
- befree-2016 importedOn "2016-02-19" NP1308042.RA2UDu1DrWssW_r6NMlUr3A-W5ZoHU4ftUqaRWPO8q3_c130_provenance.