Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP444984.RAioeFdNSKwJz7UPE9V7vwpwO5amYxYpKtivIIGm7kdic130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP444984.RAioeFdNSKwJz7UPE9V7vwpwO5amYxYpKtivIIGm7kdic130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP444984.RAioeFdNSKwJz7UPE9V7vwpwO5amYxYpKtivIIGm7kdic130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP444984.RAioeFdNSKwJz7UPE9V7vwpwO5amYxYpKtivIIGm7kdic130_provenance.
- befree-20150227 importedOn "2015-02-27" NP444984.RAioeFdNSKwJz7UPE9V7vwpwO5amYxYpKtivIIGm7kdic130_provenance.
- NP444984.RAioeFdNSKwJz7UPE9V7vwpwO5amYxYpKtivIIGm7kdic130_assertion wasGeneratedBy ECO_0000203 NP444984.RAioeFdNSKwJz7UPE9V7vwpwO5amYxYpKtivIIGm7kdic130_provenance.
- NP444984.RAioeFdNSKwJz7UPE9V7vwpwO5amYxYpKtivIIGm7kdic130_assertion wasDerivedFrom befree-20150227 NP444984.RAioeFdNSKwJz7UPE9V7vwpwO5amYxYpKtivIIGm7kdic130_provenance.
- NP444984.RAioeFdNSKwJz7UPE9V7vwpwO5amYxYpKtivIIGm7kdic130_assertion SIO_000772 23000143 NP444984.RAioeFdNSKwJz7UPE9V7vwpwO5amYxYpKtivIIGm7kdic130_provenance.
- NP444984.RAioeFdNSKwJz7UPE9V7vwpwO5amYxYpKtivIIGm7kdic130_assertion evidence source_evidence_literature NP444984.RAioeFdNSKwJz7UPE9V7vwpwO5amYxYpKtivIIGm7kdic130_provenance.
- NP444984.RAioeFdNSKwJz7UPE9V7vwpwO5amYxYpKtivIIGm7kdic130_assertion description "[A noncoding, regulatory mutation implicates HCFC1 in nonsyndromic intellectual disability.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP444984.RAioeFdNSKwJz7UPE9V7vwpwO5amYxYpKtivIIGm7kdic130_provenance.