Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP434090.RAThA0U526hrIdJRc76vLgFgx_mspOyZhS2NXKmYqrqnw130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP434090.RAThA0U526hrIdJRc76vLgFgx_mspOyZhS2NXKmYqrqnw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP434090.RAThA0U526hrIdJRc76vLgFgx_mspOyZhS2NXKmYqrqnw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP434090.RAThA0U526hrIdJRc76vLgFgx_mspOyZhS2NXKmYqrqnw130_provenance.
- NP434090.RAThA0U526hrIdJRc76vLgFgx_mspOyZhS2NXKmYqrqnw130_assertion description "[Mutations in progranulin (PGRN) are associated with frontotemporal dementia with or without parkinsonism.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP434090.RAThA0U526hrIdJRc76vLgFgx_mspOyZhS2NXKmYqrqnw130_provenance.
- NP434090.RAThA0U526hrIdJRc76vLgFgx_mspOyZhS2NXKmYqrqnw130_assertion evidence source_evidence_literature NP434090.RAThA0U526hrIdJRc76vLgFgx_mspOyZhS2NXKmYqrqnw130_provenance.
- NP434090.RAThA0U526hrIdJRc76vLgFgx_mspOyZhS2NXKmYqrqnw130_assertion SIO_000772 17949857 NP434090.RAThA0U526hrIdJRc76vLgFgx_mspOyZhS2NXKmYqrqnw130_provenance.
- NP434090.RAThA0U526hrIdJRc76vLgFgx_mspOyZhS2NXKmYqrqnw130_assertion wasDerivedFrom befree-20150227 NP434090.RAThA0U526hrIdJRc76vLgFgx_mspOyZhS2NXKmYqrqnw130_provenance.
- NP434090.RAThA0U526hrIdJRc76vLgFgx_mspOyZhS2NXKmYqrqnw130_assertion wasGeneratedBy ECO_0000203 NP434090.RAThA0U526hrIdJRc76vLgFgx_mspOyZhS2NXKmYqrqnw130_provenance.
- befree-20150227 importedOn "2015-02-27" NP434090.RAThA0U526hrIdJRc76vLgFgx_mspOyZhS2NXKmYqrqnw130_provenance.