Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP960070.RAUNWTY64A1nxa2CWzO08xf_7Hf8QTH3Kb8NQ2hmgNRUE130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP960070.RAUNWTY64A1nxa2CWzO08xf_7Hf8QTH3Kb8NQ2hmgNRUE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP960070.RAUNWTY64A1nxa2CWzO08xf_7Hf8QTH3Kb8NQ2hmgNRUE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP960070.RAUNWTY64A1nxa2CWzO08xf_7Hf8QTH3Kb8NQ2hmgNRUE130_provenance.
- NP960070.RAUNWTY64A1nxa2CWzO08xf_7Hf8QTH3Kb8NQ2hmgNRUE130_assertion description "[It also extends the phenotypical heterogeneity associated with LHX4 mutations, which includes variable anterior pituitary hormone deficits, as well as pituitary and extrapituitary abnormalities.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP960070.RAUNWTY64A1nxa2CWzO08xf_7Hf8QTH3Kb8NQ2hmgNRUE130_provenance.
- NP960070.RAUNWTY64A1nxa2CWzO08xf_7Hf8QTH3Kb8NQ2hmgNRUE130_assertion evidence source_evidence_literature NP960070.RAUNWTY64A1nxa2CWzO08xf_7Hf8QTH3Kb8NQ2hmgNRUE130_provenance.
- NP960070.RAUNWTY64A1nxa2CWzO08xf_7Hf8QTH3Kb8NQ2hmgNRUE130_assertion SIO_000772 18445675 NP960070.RAUNWTY64A1nxa2CWzO08xf_7Hf8QTH3Kb8NQ2hmgNRUE130_provenance.
- NP960070.RAUNWTY64A1nxa2CWzO08xf_7Hf8QTH3Kb8NQ2hmgNRUE130_assertion wasDerivedFrom befree-20150227 NP960070.RAUNWTY64A1nxa2CWzO08xf_7Hf8QTH3Kb8NQ2hmgNRUE130_provenance.
- NP960070.RAUNWTY64A1nxa2CWzO08xf_7Hf8QTH3Kb8NQ2hmgNRUE130_assertion wasGeneratedBy ECO_0000203 NP960070.RAUNWTY64A1nxa2CWzO08xf_7Hf8QTH3Kb8NQ2hmgNRUE130_provenance.
- befree-20150227 importedOn "2015-02-27" NP960070.RAUNWTY64A1nxa2CWzO08xf_7Hf8QTH3Kb8NQ2hmgNRUE130_provenance.