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- source_evidence_literature type ECO_0000212 NP380635.RA6Tu6i6-cUCpjUPzJrzgR9lFnqyp4E53GREp8laSbALo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP380635.RA6Tu6i6-cUCpjUPzJrzgR9lFnqyp4E53GREp8laSbALo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP380635.RA6Tu6i6-cUCpjUPzJrzgR9lFnqyp4E53GREp8laSbALo130_provenance.
- NP380635.RA6Tu6i6-cUCpjUPzJrzgR9lFnqyp4E53GREp8laSbALo130_assertion description "[Haploinsufficiency of Tbx1 is likely a major determinant of cardiac and craniofacial birth defects associated with DiGeorge syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP380635.RA6Tu6i6-cUCpjUPzJrzgR9lFnqyp4E53GREp8laSbALo130_provenance.
- NP380635.RA6Tu6i6-cUCpjUPzJrzgR9lFnqyp4E53GREp8laSbALo130_assertion evidence source_evidence_literature NP380635.RA6Tu6i6-cUCpjUPzJrzgR9lFnqyp4E53GREp8laSbALo130_provenance.
- NP380635.RA6Tu6i6-cUCpjUPzJrzgR9lFnqyp4E53GREp8laSbALo130_assertion SIO_000772 12533514 NP380635.RA6Tu6i6-cUCpjUPzJrzgR9lFnqyp4E53GREp8laSbALo130_provenance.
- NP380635.RA6Tu6i6-cUCpjUPzJrzgR9lFnqyp4E53GREp8laSbALo130_assertion wasDerivedFrom befree-2016 NP380635.RA6Tu6i6-cUCpjUPzJrzgR9lFnqyp4E53GREp8laSbALo130_provenance.
- NP380635.RA6Tu6i6-cUCpjUPzJrzgR9lFnqyp4E53GREp8laSbALo130_assertion wasGeneratedBy ECO_0000203 NP380635.RA6Tu6i6-cUCpjUPzJrzgR9lFnqyp4E53GREp8laSbALo130_provenance.
- befree-2016 importedOn "2016-02-19" NP380635.RA6Tu6i6-cUCpjUPzJrzgR9lFnqyp4E53GREp8laSbALo130_provenance.