Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP232682.RAqmVLoT_2snMrMPl24Dib3ym8Hh3GWM0LKlWbXrL7Vs4130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP232682.RAqmVLoT_2snMrMPl24Dib3ym8Hh3GWM0LKlWbXrL7Vs4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP232682.RAqmVLoT_2snMrMPl24Dib3ym8Hh3GWM0LKlWbXrL7Vs4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP232682.RAqmVLoT_2snMrMPl24Dib3ym8Hh3GWM0LKlWbXrL7Vs4130_provenance.
- NP232682.RAqmVLoT_2snMrMPl24Dib3ym8Hh3GWM0LKlWbXrL7Vs4130_assertion description "[ALK1 plays as notable a role as BMPR2 in the etiology of PAH/carriers with the ALK1 mutation within the serine - threonine kinase domain are at risk of developing PAH and hereditary hemorrhagic telangiectasia ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP232682.RAqmVLoT_2snMrMPl24Dib3ym8Hh3GWM0LKlWbXrL7Vs4130_provenance.
- NP232682.RAqmVLoT_2snMrMPl24Dib3ym8Hh3GWM0LKlWbXrL7Vs4130_assertion evidence source_evidence_literature NP232682.RAqmVLoT_2snMrMPl24Dib3ym8Hh3GWM0LKlWbXrL7Vs4130_provenance.
- NP232682.RAqmVLoT_2snMrMPl24Dib3ym8Hh3GWM0LKlWbXrL7Vs4130_assertion SIO_000772 18159113 NP232682.RAqmVLoT_2snMrMPl24Dib3ym8Hh3GWM0LKlWbXrL7Vs4130_provenance.
- NP232682.RAqmVLoT_2snMrMPl24Dib3ym8Hh3GWM0LKlWbXrL7Vs4130_assertion wasDerivedFrom lhgdn-20090331 NP232682.RAqmVLoT_2snMrMPl24Dib3ym8Hh3GWM0LKlWbXrL7Vs4130_provenance.
- NP232682.RAqmVLoT_2snMrMPl24Dib3ym8Hh3GWM0LKlWbXrL7Vs4130_assertion wasGeneratedBy ECO_0000203 NP232682.RAqmVLoT_2snMrMPl24Dib3ym8Hh3GWM0LKlWbXrL7Vs4130_provenance.
- lhgdn-20090331 importedOn "2009-03-31" NP232682.RAqmVLoT_2snMrMPl24Dib3ym8Hh3GWM0LKlWbXrL7Vs4130_provenance.