Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP896016.RAHHKsalh-nwWMgur5Qxje0VOGSIKWrT-9JIW8GMpOnLM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP896016.RAHHKsalh-nwWMgur5Qxje0VOGSIKWrT-9JIW8GMpOnLM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP896016.RAHHKsalh-nwWMgur5Qxje0VOGSIKWrT-9JIW8GMpOnLM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP896016.RAHHKsalh-nwWMgur5Qxje0VOGSIKWrT-9JIW8GMpOnLM130_provenance.
- NP896016.RAHHKsalh-nwWMgur5Qxje0VOGSIKWrT-9JIW8GMpOnLM130_assertion description "[The ZRS contains point mutations that segregate with polydactyly in four unrelated families with PPD and in the Hx mouse mutant.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP896016.RAHHKsalh-nwWMgur5Qxje0VOGSIKWrT-9JIW8GMpOnLM130_provenance.
- NP896016.RAHHKsalh-nwWMgur5Qxje0VOGSIKWrT-9JIW8GMpOnLM130_assertion evidence source_evidence_literature NP896016.RAHHKsalh-nwWMgur5Qxje0VOGSIKWrT-9JIW8GMpOnLM130_provenance.
- NP896016.RAHHKsalh-nwWMgur5Qxje0VOGSIKWrT-9JIW8GMpOnLM130_assertion SIO_000772 12837695 NP896016.RAHHKsalh-nwWMgur5Qxje0VOGSIKWrT-9JIW8GMpOnLM130_provenance.
- NP896016.RAHHKsalh-nwWMgur5Qxje0VOGSIKWrT-9JIW8GMpOnLM130_assertion wasDerivedFrom befree-20150227 NP896016.RAHHKsalh-nwWMgur5Qxje0VOGSIKWrT-9JIW8GMpOnLM130_provenance.
- NP896016.RAHHKsalh-nwWMgur5Qxje0VOGSIKWrT-9JIW8GMpOnLM130_assertion wasGeneratedBy ECO_0000203 NP896016.RAHHKsalh-nwWMgur5Qxje0VOGSIKWrT-9JIW8GMpOnLM130_provenance.
- befree-20150227 importedOn "2015-02-27" NP896016.RAHHKsalh-nwWMgur5Qxje0VOGSIKWrT-9JIW8GMpOnLM130_provenance.