Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP467541.RAU4KZPiD9AMBaRGnYQ7E9oC-Iya9NqY5SAlEc3aX7KsE130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP467541.RAU4KZPiD9AMBaRGnYQ7E9oC-Iya9NqY5SAlEc3aX7KsE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP467541.RAU4KZPiD9AMBaRGnYQ7E9oC-Iya9NqY5SAlEc3aX7KsE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP467541.RAU4KZPiD9AMBaRGnYQ7E9oC-Iya9NqY5SAlEc3aX7KsE130_provenance.
- NP467541.RAU4KZPiD9AMBaRGnYQ7E9oC-Iya9NqY5SAlEc3aX7KsE130_assertion wasGeneratedBy ECO_0000203 NP467541.RAU4KZPiD9AMBaRGnYQ7E9oC-Iya9NqY5SAlEc3aX7KsE130_provenance.
- NP467541.RAU4KZPiD9AMBaRGnYQ7E9oC-Iya9NqY5SAlEc3aX7KsE130_assertion wasDerivedFrom befree-20140225 NP467541.RAU4KZPiD9AMBaRGnYQ7E9oC-Iya9NqY5SAlEc3aX7KsE130_provenance.
- NP467541.RAU4KZPiD9AMBaRGnYQ7E9oC-Iya9NqY5SAlEc3aX7KsE130_assertion SIO_000772 10816131 NP467541.RAU4KZPiD9AMBaRGnYQ7E9oC-Iya9NqY5SAlEc3aX7KsE130_provenance.
- NP467541.RAU4KZPiD9AMBaRGnYQ7E9oC-Iya9NqY5SAlEc3aX7KsE130_assertion evidence source_evidence_literature NP467541.RAU4KZPiD9AMBaRGnYQ7E9oC-Iya9NqY5SAlEc3aX7KsE130_provenance.
- NP467541.RAU4KZPiD9AMBaRGnYQ7E9oC-Iya9NqY5SAlEc3aX7KsE130_assertion description "[However, the frequency of the HLA-G insertion/deletion polymorphism in exon 8 deviated significantly from Hardy-Weinberg expectations in PE off-spring, reflecting an excess of heterozygotes for these polymorphisms in PE offspring.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP467541.RAU4KZPiD9AMBaRGnYQ7E9oC-Iya9NqY5SAlEc3aX7KsE130_provenance.
- befree-20140225 importedOn "2014-02-25" NP467541.RAU4KZPiD9AMBaRGnYQ7E9oC-Iya9NqY5SAlEc3aX7KsE130_provenance.