Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP750610.RA68kR0lXqI0GMKPxSBBV9IOuMCR8uKgvVrBIHLvHmMZ8130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP750610.RA68kR0lXqI0GMKPxSBBV9IOuMCR8uKgvVrBIHLvHmMZ8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP750610.RA68kR0lXqI0GMKPxSBBV9IOuMCR8uKgvVrBIHLvHmMZ8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP750610.RA68kR0lXqI0GMKPxSBBV9IOuMCR8uKgvVrBIHLvHmMZ8130_provenance.
- befree-2016 importedOn "2016-02-19" NP750610.RA68kR0lXqI0GMKPxSBBV9IOuMCR8uKgvVrBIHLvHmMZ8130_provenance.
- NP750610.RA68kR0lXqI0GMKPxSBBV9IOuMCR8uKgvVrBIHLvHmMZ8130_assertion wasGeneratedBy ECO_0000203 NP750610.RA68kR0lXqI0GMKPxSBBV9IOuMCR8uKgvVrBIHLvHmMZ8130_provenance.
- NP750610.RA68kR0lXqI0GMKPxSBBV9IOuMCR8uKgvVrBIHLvHmMZ8130_assertion wasDerivedFrom befree-2016 NP750610.RA68kR0lXqI0GMKPxSBBV9IOuMCR8uKgvVrBIHLvHmMZ8130_provenance.
- NP750610.RA68kR0lXqI0GMKPxSBBV9IOuMCR8uKgvVrBIHLvHmMZ8130_assertion SIO_000772 19592504 NP750610.RA68kR0lXqI0GMKPxSBBV9IOuMCR8uKgvVrBIHLvHmMZ8130_provenance.
- NP750610.RA68kR0lXqI0GMKPxSBBV9IOuMCR8uKgvVrBIHLvHmMZ8130_assertion evidence source_evidence_literature NP750610.RA68kR0lXqI0GMKPxSBBV9IOuMCR8uKgvVrBIHLvHmMZ8130_provenance.
- NP750610.RA68kR0lXqI0GMKPxSBBV9IOuMCR8uKgvVrBIHLvHmMZ8130_assertion description "[MDR analysis for intragenic mutations of FOXL2 gene reported in previous BPES studies indicated that the mutations which led to much stronger disturbance of amino acid sequence were responsible for more type I BPES, while other kinds of mutation were responsible for more type II BPES.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP750610.RA68kR0lXqI0GMKPxSBBV9IOuMCR8uKgvVrBIHLvHmMZ8130_provenance.