Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP713107.RAFDRwwIbIeOo0aBfR1NXbiWV-WbkfKrYEBRTG7mHHN4o130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP713107.RAFDRwwIbIeOo0aBfR1NXbiWV-WbkfKrYEBRTG7mHHN4o130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP713107.RAFDRwwIbIeOo0aBfR1NXbiWV-WbkfKrYEBRTG7mHHN4o130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP713107.RAFDRwwIbIeOo0aBfR1NXbiWV-WbkfKrYEBRTG7mHHN4o130_provenance.
- NP713107.RAFDRwwIbIeOo0aBfR1NXbiWV-WbkfKrYEBRTG7mHHN4o130_assertion description "[The genetic basis for XX true hermaphroditism and sex reversal syndromes unrelated to SRY translocation is still mostly unclear.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP713107.RAFDRwwIbIeOo0aBfR1NXbiWV-WbkfKrYEBRTG7mHHN4o130_provenance.
- NP713107.RAFDRwwIbIeOo0aBfR1NXbiWV-WbkfKrYEBRTG7mHHN4o130_assertion evidence source_evidence_literature NP713107.RAFDRwwIbIeOo0aBfR1NXbiWV-WbkfKrYEBRTG7mHHN4o130_provenance.
- NP713107.RAFDRwwIbIeOo0aBfR1NXbiWV-WbkfKrYEBRTG7mHHN4o130_assertion SIO_000772 18085567 NP713107.RAFDRwwIbIeOo0aBfR1NXbiWV-WbkfKrYEBRTG7mHHN4o130_provenance.
- NP713107.RAFDRwwIbIeOo0aBfR1NXbiWV-WbkfKrYEBRTG7mHHN4o130_assertion wasDerivedFrom befree-20150227 NP713107.RAFDRwwIbIeOo0aBfR1NXbiWV-WbkfKrYEBRTG7mHHN4o130_provenance.
- NP713107.RAFDRwwIbIeOo0aBfR1NXbiWV-WbkfKrYEBRTG7mHHN4o130_assertion wasGeneratedBy ECO_0000203 NP713107.RAFDRwwIbIeOo0aBfR1NXbiWV-WbkfKrYEBRTG7mHHN4o130_provenance.
- befree-20150227 importedOn "2015-02-27" NP713107.RAFDRwwIbIeOo0aBfR1NXbiWV-WbkfKrYEBRTG7mHHN4o130_provenance.