Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP704779.RA6ZgkHMIhiINuWN8vVDvct5u18WaTUBa2McILSsN2kr4130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP704779.RA6ZgkHMIhiINuWN8vVDvct5u18WaTUBa2McILSsN2kr4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP704779.RA6ZgkHMIhiINuWN8vVDvct5u18WaTUBa2McILSsN2kr4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP704779.RA6ZgkHMIhiINuWN8vVDvct5u18WaTUBa2McILSsN2kr4130_provenance.
- NP704779.RA6ZgkHMIhiINuWN8vVDvct5u18WaTUBa2McILSsN2kr4130_assertion description "[The molecular defects of NS are genetically heterogeneous and involve several genes other than PTPN11 related to the RAS-MAPK pathway.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP704779.RA6ZgkHMIhiINuWN8vVDvct5u18WaTUBa2McILSsN2kr4130_provenance.
- NP704779.RA6ZgkHMIhiINuWN8vVDvct5u18WaTUBa2McILSsN2kr4130_assertion evidence source_evidence_literature NP704779.RA6ZgkHMIhiINuWN8vVDvct5u18WaTUBa2McILSsN2kr4130_provenance.
- NP704779.RA6ZgkHMIhiINuWN8vVDvct5u18WaTUBa2McILSsN2kr4130_assertion SIO_000772 19020799 NP704779.RA6ZgkHMIhiINuWN8vVDvct5u18WaTUBa2McILSsN2kr4130_provenance.
- NP704779.RA6ZgkHMIhiINuWN8vVDvct5u18WaTUBa2McILSsN2kr4130_assertion wasDerivedFrom befree-2016 NP704779.RA6ZgkHMIhiINuWN8vVDvct5u18WaTUBa2McILSsN2kr4130_provenance.
- NP704779.RA6ZgkHMIhiINuWN8vVDvct5u18WaTUBa2McILSsN2kr4130_assertion wasGeneratedBy ECO_0000203 NP704779.RA6ZgkHMIhiINuWN8vVDvct5u18WaTUBa2McILSsN2kr4130_provenance.
- befree-2016 importedOn "2016-02-19" NP704779.RA6ZgkHMIhiINuWN8vVDvct5u18WaTUBa2McILSsN2kr4130_provenance.