Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1399623.RAkk1YnfP6zxO9k_Tznzeu6y829WUf8SmOroKglplaI6Y130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP1399623.RAkk1YnfP6zxO9k_Tznzeu6y829WUf8SmOroKglplaI6Y130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1399623.RAkk1YnfP6zxO9k_Tznzeu6y829WUf8SmOroKglplaI6Y130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1399623.RAkk1YnfP6zxO9k_Tznzeu6y829WUf8SmOroKglplaI6Y130_provenance.
- NP1399623.RAkk1YnfP6zxO9k_Tznzeu6y829WUf8SmOroKglplaI6Y130_assertion description "[Detailed clinical descriptions and genetic analysis of patients with phenotypes intermediate between HPD/DRD (mild) and GCH-deficient HPA (severe) have not been reported.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1399623.RAkk1YnfP6zxO9k_Tznzeu6y829WUf8SmOroKglplaI6Y130_provenance.
- NP1399623.RAkk1YnfP6zxO9k_Tznzeu6y829WUf8SmOroKglplaI6Y130_assertion evidence source_evidence_literature NP1399623.RAkk1YnfP6zxO9k_Tznzeu6y829WUf8SmOroKglplaI6Y130_provenance.
- NP1399623.RAkk1YnfP6zxO9k_Tznzeu6y829WUf8SmOroKglplaI6Y130_assertion SIO_000772 9667588 NP1399623.RAkk1YnfP6zxO9k_Tznzeu6y829WUf8SmOroKglplaI6Y130_provenance.
- NP1399623.RAkk1YnfP6zxO9k_Tznzeu6y829WUf8SmOroKglplaI6Y130_assertion wasDerivedFrom befree-2016 NP1399623.RAkk1YnfP6zxO9k_Tznzeu6y829WUf8SmOroKglplaI6Y130_provenance.
- NP1399623.RAkk1YnfP6zxO9k_Tznzeu6y829WUf8SmOroKglplaI6Y130_assertion wasGeneratedBy ECO_0000203 NP1399623.RAkk1YnfP6zxO9k_Tznzeu6y829WUf8SmOroKglplaI6Y130_provenance.
- befree-2016 importedOn "2016-02-19" NP1399623.RAkk1YnfP6zxO9k_Tznzeu6y829WUf8SmOroKglplaI6Y130_provenance.