Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP504318.RA8EODpEFPoimLtRdl0AstlcC1eplGeUNIyrQNDqxKLoQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP504318.RA8EODpEFPoimLtRdl0AstlcC1eplGeUNIyrQNDqxKLoQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP504318.RA8EODpEFPoimLtRdl0AstlcC1eplGeUNIyrQNDqxKLoQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP504318.RA8EODpEFPoimLtRdl0AstlcC1eplGeUNIyrQNDqxKLoQ130_provenance.
- befree-20150227 importedOn "2015-02-27" NP504318.RA8EODpEFPoimLtRdl0AstlcC1eplGeUNIyrQNDqxKLoQ130_provenance.
- NP504318.RA8EODpEFPoimLtRdl0AstlcC1eplGeUNIyrQNDqxKLoQ130_assertion wasGeneratedBy ECO_0000203 NP504318.RA8EODpEFPoimLtRdl0AstlcC1eplGeUNIyrQNDqxKLoQ130_provenance.
- NP504318.RA8EODpEFPoimLtRdl0AstlcC1eplGeUNIyrQNDqxKLoQ130_assertion wasDerivedFrom befree-20150227 NP504318.RA8EODpEFPoimLtRdl0AstlcC1eplGeUNIyrQNDqxKLoQ130_provenance.
- NP504318.RA8EODpEFPoimLtRdl0AstlcC1eplGeUNIyrQNDqxKLoQ130_assertion SIO_000772 22310223 NP504318.RA8EODpEFPoimLtRdl0AstlcC1eplGeUNIyrQNDqxKLoQ130_provenance.
- NP504318.RA8EODpEFPoimLtRdl0AstlcC1eplGeUNIyrQNDqxKLoQ130_assertion evidence source_evidence_literature NP504318.RA8EODpEFPoimLtRdl0AstlcC1eplGeUNIyrQNDqxKLoQ130_provenance.
- NP504318.RA8EODpEFPoimLtRdl0AstlcC1eplGeUNIyrQNDqxKLoQ130_assertion description "[Utilizing prospective sequence analysis of SHH, ZIC2, SIX3 and TGIF in holoprosencephaly probands to describe the parameters limiting the observed frequency of mutant gene×gene interactions.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP504318.RA8EODpEFPoimLtRdl0AstlcC1eplGeUNIyrQNDqxKLoQ130_provenance.