Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP691587.RASM4jA49M3EM_rhUj9rCG3NX2GmgGvBUfsUY3l3DtV8E130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP691587.RASM4jA49M3EM_rhUj9rCG3NX2GmgGvBUfsUY3l3DtV8E130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP691587.RASM4jA49M3EM_rhUj9rCG3NX2GmgGvBUfsUY3l3DtV8E130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP691587.RASM4jA49M3EM_rhUj9rCG3NX2GmgGvBUfsUY3l3DtV8E130_provenance.
- NP691587.RASM4jA49M3EM_rhUj9rCG3NX2GmgGvBUfsUY3l3DtV8E130_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." NP691587.RASM4jA49M3EM_rhUj9rCG3NX2GmgGvBUfsUY3l3DtV8E130_provenance.
- NP691587.RASM4jA49M3EM_rhUj9rCG3NX2GmgGvBUfsUY3l3DtV8E130_assertion evidence source_evidence_literature NP691587.RASM4jA49M3EM_rhUj9rCG3NX2GmgGvBUfsUY3l3DtV8E130_provenance.
- NP691587.RASM4jA49M3EM_rhUj9rCG3NX2GmgGvBUfsUY3l3DtV8E130_assertion SIO_000772 10493923 NP691587.RASM4jA49M3EM_rhUj9rCG3NX2GmgGvBUfsUY3l3DtV8E130_provenance.
- NP691587.RASM4jA49M3EM_rhUj9rCG3NX2GmgGvBUfsUY3l3DtV8E130_assertion wasDerivedFrom befree-20150227 NP691587.RASM4jA49M3EM_rhUj9rCG3NX2GmgGvBUfsUY3l3DtV8E130_provenance.
- NP691587.RASM4jA49M3EM_rhUj9rCG3NX2GmgGvBUfsUY3l3DtV8E130_assertion wasGeneratedBy ECO_0000203 NP691587.RASM4jA49M3EM_rhUj9rCG3NX2GmgGvBUfsUY3l3DtV8E130_provenance.
- befree-20150227 importedOn "2015-02-27" NP691587.RASM4jA49M3EM_rhUj9rCG3NX2GmgGvBUfsUY3l3DtV8E130_provenance.