Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP904963.RA0fcgom-v4cbdDkzxk1jYpbtXgRo3tZnDeBfkRNxltuI130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP904963.RA0fcgom-v4cbdDkzxk1jYpbtXgRo3tZnDeBfkRNxltuI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP904963.RA0fcgom-v4cbdDkzxk1jYpbtXgRo3tZnDeBfkRNxltuI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP904963.RA0fcgom-v4cbdDkzxk1jYpbtXgRo3tZnDeBfkRNxltuI130_provenance.
- NP904963.RA0fcgom-v4cbdDkzxk1jYpbtXgRo3tZnDeBfkRNxltuI130_assertion description "[Heterozygous and homozygous mutations in PITX3 in a large Lebanese family with posterior polar cataracts and neurodevelopmental abnormalities.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP904963.RA0fcgom-v4cbdDkzxk1jYpbtXgRo3tZnDeBfkRNxltuI130_provenance.
- NP904963.RA0fcgom-v4cbdDkzxk1jYpbtXgRo3tZnDeBfkRNxltuI130_assertion evidence source_evidence_literature NP904963.RA0fcgom-v4cbdDkzxk1jYpbtXgRo3tZnDeBfkRNxltuI130_provenance.
- NP904963.RA0fcgom-v4cbdDkzxk1jYpbtXgRo3tZnDeBfkRNxltuI130_assertion SIO_000772 16565358 NP904963.RA0fcgom-v4cbdDkzxk1jYpbtXgRo3tZnDeBfkRNxltuI130_provenance.
- NP904963.RA0fcgom-v4cbdDkzxk1jYpbtXgRo3tZnDeBfkRNxltuI130_assertion wasDerivedFrom befree-20140225 NP904963.RA0fcgom-v4cbdDkzxk1jYpbtXgRo3tZnDeBfkRNxltuI130_provenance.
- NP904963.RA0fcgom-v4cbdDkzxk1jYpbtXgRo3tZnDeBfkRNxltuI130_assertion wasGeneratedBy ECO_0000203 NP904963.RA0fcgom-v4cbdDkzxk1jYpbtXgRo3tZnDeBfkRNxltuI130_provenance.
- befree-20140225 importedOn "2014-02-25" NP904963.RA0fcgom-v4cbdDkzxk1jYpbtXgRo3tZnDeBfkRNxltuI130_provenance.