Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP591018.RAC1Th0KJ3RFaszDnmjXWEzSUtA__FnydiLnkuco8cCto130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP591018.RAC1Th0KJ3RFaszDnmjXWEzSUtA__FnydiLnkuco8cCto130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP591018.RAC1Th0KJ3RFaszDnmjXWEzSUtA__FnydiLnkuco8cCto130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP591018.RAC1Th0KJ3RFaszDnmjXWEzSUtA__FnydiLnkuco8cCto130_provenance.
- NP591018.RAC1Th0KJ3RFaszDnmjXWEzSUtA__FnydiLnkuco8cCto130_assertion description "[Although the relative abundance of the deletion form of SP-B mRNA remains constant among normal lungs, it is found with relatively higher abundance in the lungs of some individuals with diseases such as congenital alveolar proteinosis, respiratory distress syndrome, bronchopulmonary dysplasia, alveolar capillary dysplasia and hypophosphatasia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP591018.RAC1Th0KJ3RFaszDnmjXWEzSUtA__FnydiLnkuco8cCto130_provenance.
- NP591018.RAC1Th0KJ3RFaszDnmjXWEzSUtA__FnydiLnkuco8cCto130_assertion evidence source_evidence_literature NP591018.RAC1Th0KJ3RFaszDnmjXWEzSUtA__FnydiLnkuco8cCto130_provenance.
- NP591018.RAC1Th0KJ3RFaszDnmjXWEzSUtA__FnydiLnkuco8cCto130_assertion SIO_000772 10493923 NP591018.RAC1Th0KJ3RFaszDnmjXWEzSUtA__FnydiLnkuco8cCto130_provenance.
- NP591018.RAC1Th0KJ3RFaszDnmjXWEzSUtA__FnydiLnkuco8cCto130_assertion wasDerivedFrom befree-20140225 NP591018.RAC1Th0KJ3RFaszDnmjXWEzSUtA__FnydiLnkuco8cCto130_provenance.
- NP591018.RAC1Th0KJ3RFaszDnmjXWEzSUtA__FnydiLnkuco8cCto130_assertion wasGeneratedBy ECO_0000203 NP591018.RAC1Th0KJ3RFaszDnmjXWEzSUtA__FnydiLnkuco8cCto130_provenance.
- befree-20140225 importedOn "2014-02-25" NP591018.RAC1Th0KJ3RFaszDnmjXWEzSUtA__FnydiLnkuco8cCto130_provenance.